Compositions And Methods Comprising Variant Microbial Proteases

ABSTRACT

The present invention provides methods for protein engineering. Specifically, the invention provides methods utilizing site evaluation libraries to design libraries that optimize two or more properties of a protein. The present invention also provides variant subtilisins suitable for various uses.

FIELD OF THE INVENTION

The present invention provides methods for protein engineering and variant proteases. Specifically, the invention provides methods utilizing site evaluation libraries. The present invention also provides subtilisin variants suitable for various uses.

BACKGROUND OF THE INVENTION

Serine proteases are a subgroup of carbonyl hydrolases comprising a diverse class of enzymes having a wide range of specificities and biological functions. Much research has been conducted on the subtilisins, due largely to their usefulness in cleaning and feed applications. Additional work has been focused on the adverse environmental conditions (e.g., exposure to oxidative agents, chelating agents, extremes of temperature and/or pH) which can adversely impact the functionality of these enzymes in various applications. Nonetheless, there remains a need in the art for enzyme systems that are able to resist these adverse conditions and retain or have improved activity over those currently known in the art.

Various protein engineering methods are known to those in the art. In general, proteins are modified in order to obtain desired protein properties. In most methods, the nucleotide sequence of a cloned gene encoding a protein is mutated and the modified gene is expressed to produce mutants, which are screened for activities of interest. Often, the mutant properties are compared with the properties of wild-type protein.

Historically, the protein design process has been approached as equivalent to the problem of finding in all of protein space the one best sequence for the desired application. This problem is extremely difficult and is “NP hard.” In complexity theory, problems defined as being in class P, are considered easy and efficient, polynomial-time algorithms exist for their solution. NP-hard problems are problems for which efficient polynomial-time algorithms are not currently known, and if any NP-hard problem could be solved, all NP-hard problems could be solved (See e.g., Pierce and Winfree, Protein Engineer., 15:779-782 [2002]). Current strategies for building and screening libraries generally involve generating protein sequence diversity randomly across the whole sequence or in controlled random fashion at defined positions within the protein. These libraries generally have a large number of members that are “negative” with respect to the primary property of interest, and require large numbers be screened in order to find the relatively small numbers of positive mutations. Generally, negative mutations are ignored, and sequence information is only obtained for the positive members.

Saturation mutagenesis (Estell et al., in World Biotech Report 1984, vol. 2: USA, Online Publications, London [1984], pages 181-187; and Wells et al., Gene 34:315-323 [1985]) is one technique that can be used to search protein space for mutations that optimize several properties in a protein. Several groups have developed strategies for identifying sites to be changed by saturation mutagenesis (Reetz et al., Agnew. Chem. Int. Edn., 44:4192-4196 [2005]; Kato et al., J. Mol. Biol., 351:683-692 [2005]; and Sandberg et al., Proc. Natl. Acad. Sci., 90:8367-8371 [1993]), but no general system for site identification has been proposed.

In addition, because most protein engineering methods produce a great number of amino acid mutation options, screening of a large number of variants generally is required to produce a desired protein property. Generally, screening is repeated over and over to produce a beneficial variant. Thus, most methods are laborious and time-consuming. There is a continuing need in the art for protein engineering methods that are efficient and produce the desired results.

SUMMARY OF THE INVENTION

The present invention provides methods for protein engineering. Specifically, the invention provides methods utilizing site evaluation libraries. In particular, the present invention provides means to use information obtained about a number of desired properties, in order to rationally and efficiently design libraries that will optimize those properties. In some embodiments, the present invention provides means to design libraries that are improved for at least two desired properties.

The present invention provides means to identify positions within an amino acid sequence of a protein that are relevant in improving desired properties of the protein. In some particularly preferred embodiments, the present invention provides means to determine which mutations are desirable in order to produce proteins with these desired properties, as well as improved properties. In some additional particularly preferred embodiments, the present invention provides means to identify amino acid positions and mutations that have improvements of a particular percentage better than the wild-type protein (e.g., better than 110% of the wild-type for one property). In still further preferred embodiments, the present invention provides means to identify mutations that provide at least one much improved property and at least one additional property that is not significantly worse than the wild-type protein (e.g., better than 110% of wild-type for one property, yet not worse than 90% of wild-type for another property). In yet further preferred embodiments, libraries are constructed based on this information. In some embodiments, the libraries are constructed using all of the identified mutations, while in some other embodiments, the libraries are constructed using a subset of the identified mutations. Indeed, it is not intended that the libraries be constrained to any particular number and/or type of mutations.

The present invention provides methods for protein engineering comprising the steps of: providing a library of protein variants; testing the library of protein variants for at least one property of interest in a test of interest; identifying a range of values for said the at least one property of interest; identifying a minimum within the range of values that is associated with a favorable outcome in the test of interest; and providing a plurality of protein variants having at least one mutation above said minimum in the range of the at least one property of interest, thereby providing a library of protein variants comprising at least one mutation, and wherein the library is enriched in members having a favorable outcome in the test of interest. In some embodiments, the favorable outcome corresponds to a value of greater than about 50%, about 60%, about 70%, about 80%, about 90%, or about 95% of a maximal value observed in the test set forth in the first step above. In some alternative embodiments, more than one test of interest is used in the methods of the present invention. In some preferred embodiments, the protein is an enzyme. In some particularly preferred embodiments, the enzyme is selected from proteases, transferases, metalloproteases, esterases, amylases, cellulases, oxidases, cutinases, and lipases.

The present invention also provides methods for protein engineering comprising the steps of: providing a library of protein variants; testing the library of protein variants for at least two properties of interest in a test of interest; identifying a range of values for the at least two properties of interest; identifying a minimum within the range of values that is associated with a favorable outcome in the test of interest; and providing a plurality of protein variants above the minimum of the range of the at least two properties of interest, thereby providing a library of protein variants enriched in members having the favorable outcome in the test of interest. In some preferred embodiments, the favorable outcome corresponds to a value of greater than about 50%, about 60%, about 70%, about 80%, about 90%, or about 95% of a maximal value observed in the test set forth in the first step above. In some preferred embodiments, the protein is an enzyme. In some particularly preferred embodiments, the enzyme is selected from proteases, transferases, metalloproteases, esterases, amylases, cellulases, oxidases, cutinases, and lipases.

The present invention also provides methods for protein engineering comprising the steps of: providing a wild-type protein and a library of protein variants of the wild-type protein; testing the library of protein variants and the wild-type protein for at least one property of interest in a test of interest; identifying a range of values for the at least one property of interest; identifying a minimum within the range of values that is associated with a favorable outcome in the test of interest; identifying the protein variants having a favorable outcome as compared to the results obtained for the wild-type, wherein the favorable outcome is an improved property of interest; and providing a plurality of protein variants above the minimum of the range of the at least one property of interest, thereby providing a library of improved protein variants enriched in members having the favorable outcome in the test of interest. In some preferred embodiments, the methods further comprise the step of determining the performance index, wherein the performance index is determined by dividing the value obtained for each of the improved protein variants and the value obtained for the wild-type protein. In some particularly preferred embodiments, the methods further comprise the step of identifying the improved protein variants, wherein the improved protein variants achieve performance index values greater than 1.1 in the test of interest. In some additional embodiments, the protein is an enzyme. In some particularly preferred embodiments, the enzyme is selected from proteases, transferases, metalloproteases, esterases, amylases, cellulases, oxidases, cutinases, and lipases. In some alternative embodiments, the protein is selected from antibodies and growth factors. In still additional preferred embodiments, the wild-type protein is a mature form an enzyme selected from proteases, transferases, metalloproteases, esterases, amylases, cellulases, oxidases, cutinases, and lipases. In some preferred embodiments, the property of interest is selected from charge, wash performance, hard surface cleaning performance, solubility, thermal stability, storage stability, detergent stability, substrate binding, enzyme inhibition, expression level, reaction rate, and substrate degradation. In some embodiments, the wild-type protein and the protein variant are components of at least one detergent composition. In some preferred embodiments, wash performance is tested in a detergent composition formulated into a powdered or liquid detergent having a pH of between 5 and 12.0.

The present invention also provides methods for producing an improved variant of a parent protein within a protein fold, comprising: assaying multiple variants of a test protein within the protein fold spanning a range of a property of interest in an assay of interest; identifying a minimum within the range of the property of interest that is associated with a favorable outcome in the assay of interest; assaying a parent protein of the protein fold in the assay of interest; and producing an improved variant of the parent protein by introducing an amino acid substitution is the parent protein such that the improved variant is above the minimum of the range of the property of interest. In some preferred embodiments, the parent protein and the test protein are different. In some embodiments, the methods further comprise the step of determining the performance index, wherein the performance index is determined by dividing the value obtained for the improved protein variant and the value obtained for the parent protein. In some embodiments, the test proteins and the parent proteins are enzymes. In some particularly preferred embodiments, the enzymes are selected from proteases, transferases, metalloproteases, esterases, amylases, cellulases, oxidases, cutinases, and lipases. In some alternative embodiments, the test and parent proteins are selected from antibodies and growth factors. In still additional preferred embodiments, the parent protein is a mature form an enzyme selected from proteases, transferases, metalloproteases, esterases, amylases, cellulases, oxidases, cutinases, and lipases. In some preferred embodiments, the property of interest is selected from charge, wash performance, hard surface cleaning performance, thermal stability, solubility, storage stability, detergent stability, substrate binding, enzyme inhibition, expression level, reaction rate, and substrate degradation. In some embodiments, the test and parent proteins are components of at least one detergent composition. In some alternative embodiment, the improved protein variant is a component of a detergent composition. In some preferred embodiments, wash performance is tested in a detergent composition formulated into a powdered or liquid detergent having a pH of between about 5 and about 12.0.

The present invention also provides isolated subtilisin variants of a Bacillus subtilisin, wherein the subtilisin variant is a mature form having proteolytic activity and comprising a substitution at one or more positions selected from positions: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 33, 35, 36, 37, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 62, 65, 66, 67, 71, 72, 73, 76, 77, 78, 79, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 101, 102, 103, 104, 105, 106, 107, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 139, 141, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 156, 157, 158, 159, 160, 162, 163, 164, 165, 166, 167, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 194, 195, 196, 197, 198, 199, 200, 201, 203, 204, 206, 207, 209, 210, 212, 213, 214, 215, 216, 217, 218, 219, 220, 222, 223, 224, 225, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 267, 268, 269, 270, 271, 272, 273 and 274, wherein the positions are numbered by correspondence with the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2. In some embodiments, the one or more positions are selected from: 1, 2, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 21, 22, 23, 24, 25, 26, 28, 29, 30, 31, 33, 35, 36, 37, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 62, 65, 66, 67, 71, 72, 73, 77, 78, 79, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 101, 102, 103, 104, 105, 106, 107, 109, 110, 111, 112, 113, 114, 115, 116, 118, 119, 122, 123, 124, 125, 126, 127, 128, 129, 131, 133, 134, 135, 136, 137, 139, 141, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 156, 157, 158, 159, 160, 162, 163, 164, 165, 166, 167, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 194, 195, 196, 197, 198, 199, 200, 201, 203, 204, 206, 207, 212, 213, 214, 215, 216, 217, 218, 219, 220, 222, 223, 224, 225, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 267, 268, 269, 270, 271, 272, 273 and 274, and wherein the positions are numbered by correspondence with the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2. In some further embodiments, the one or more positions are selected from: 2, 3, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 19, 20, 21, 21, 22, 23, 25, 26, 28, 29, 30, 31, 33, 35, 36, 37, 39, 40, 41, 42, 44, 46, 47, 48, 49, 50, 51, 53, 54, 55, 56, 57, 58, 59, 60, 62, 65, 66, 67, 71, 73, 77, 78, 79, 81, 82, 83, 84, 85, 86, 88, 89, 90, 91, 92, 93, 94, 95, 96, 102, 105, 106, 110, 111, 112, 113, 114, 115, 116, 122, 123, 124, 125, 126, 128, 129, 131, 133, 134, 135, 136, 137, 139, 141, 143, 145, 146, 147, 148, 149, 150, 151, 152, 153, 156, 157, 158, 159, 160, 162, 165, 166, 167, 169, 170, 171, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 186, 187, 189, 190, 191, 192, 194, 195, 196, 197, 198, 199, 200, 201, 203, 204, 206, 207, 212, 214, 216, 217, 218, 219, 220, 222, 223, 224, 225, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 249, 250, 251, 253, 254, 255, 257, 258, 259, 260, 261, 262, 263, 264, 265, 267, 268, 269, 270, 271, 272, 273, and 274, and wherein the positions are numbered by correspondence with the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2. In some embodiments, the subtilisin variant further comprises a substitution at one or more positions selected from 18, 52, 72, 117, 119, 127, 144, 185, 209 and 213, and wherein the positions are numbered by correspondence with the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2. In some preferred embodiments, the substitution comprises one or more of the positions: A001C, A001D, A001E, A001F, A001G, A001H, A001I, A001K, A001L, A001M, A001N, A001Q, A001R, A001S, A001V, A001W, Q002A, Q002D, Q002E, Q002G, Q002S, S003A, S003D, S003F, S003G, S003I, S003K, S003L, S003M, S003N, S003P, S003Q, S003R, S003T, S003V, S003W, S003Y, P005C, P005E, P005G, P005N, P005Q, P005T, Y006A, Y006C, Y006E, Y006F, Y006G, Y006K, Y006M, Y006N, Y006P, Y006Q, Y006R, Y006T, Y006V, Y006W, S009A, S009C, S009E, S009F, S009G, S009H, S009K, S009L, S009M, S009P, S009Q, S009R, S009T, S009V, S009W, Q010A, Q010C, Q010E, Q010F, Q010G, Q010H, Q010I, Q010K, Q010L, Q010M, Q010R, Q010S, Q010T, Q010V, Q010W, I011C, I011L, I011T, I011y, I011Y, K012A, K012C, K012D, K012E, K012F, K012G, K012H, K012I, K012N, K012Q, K012S, K012T, K012V, K012W, K012Y, A013C, A013F, A013G, A013H, A013L, A013R, A013S, A013T, A013V, P014A, P014C, P014D, P014E, P014F, P014G, P014I, P014K, P014L, P014M, P014N, P014Q, P014R, P014S, P014T, P014V, P014W, P014Y, A015C, A015D, A015E, A015F, A015G, A015H, A015I, A015K, A015L, A015M, A015P, A015Q, A015R, A015T, A015V, A015Y, L016A, L016C, L016I, L016M, L016Q, L016S, L016T, H017F, H017I, H017L, H017M, H017V, H017W, H017Y, S018A, S018E, S018F, S018G, S018H, S018I, S018K, S018L, S018M, S018N, S018P, S018Q, S018R, S018T, S018V, S018W, S018Y, Q019A, Q019C, Q019D, Q019E, Q019G, Q019I, Q019K, Q019M, Q019R, Q019T, Q019V, G020A, G020C, G020D, G020E, G020F, G020H, G020K, G020M, G020N, G020P, G020Q, G020R, G020S, G020W, Y021A, Y021C, Y021D, Y021E, Y021F, Y021G, Y021H, Y021K, Y021M, Y021R, Y021S, Y021T, Y021V, Y021W, T022A, T022C, T022E, T022F, T022G, T022H, T022I, T022K, T022L, T022M, T022N, T022Q, T022S, T022V, T022W, T022Y, S024C, S024F, S024G, S024H, S024I, S024K, S024L, S024M, S024N, S024Q, S024R, S024T, S024W, S024Y, N025C, N025E, N025F, N025G, N025H, N025I, N025K, N025L, N025M, N025P, N025R, N025S, N025T, N025V, N025W, K027A, K027D, K027E, K027F, K027G, K027H, K027L, K027M, K027P, K027R, K027S, K027W, K027Y, S033A, S033F, S033G, S033H, S033P, S033T, S033W, I035A, I035C, I035D, I035R, I035S, I035T, I035V, D036A, D036C, D036E, D036Q, D036S, D036W, S037A, S037C, S037E, S037F, S037G, S037H, S037K, S037L, S037M, S037P, S037Q, S037R, S037T, S037W, H039C, H039Q, H039T, H039V, P040A, P040C, P040E, P040F, P040G, P040G, P040H, P040I, P040K, P040L, P040M, P040N, P040Q, P040R, P040S, P040T, P040V, P040W, D041E, L042I, L042M, L042V, K043A, K043C, K043D, K043E, K043F, K043G, K043I, K043L, K043M, K043N, K043R, K043S, K043T, K043V, K043W, K043Y, V044A, V044C, V044I, V044L, V044M, V044P, V044S, V044T, A045C, A045E, A045F, A045H, A045I, A045K, A045L, A045M, A045N, A045P, A045Q, A045S, A045T, A045V, A045Y, G046A, G046C, G046E, G046H, G046K, G046M, G046N, G046Q, G046T, G046W, G046Y, A048C, A048D, A048E, A048F, A048H, A048I, A048K, A048L, A048M, A048Q, A048R, A048S, A048T, A048V, A048W, A048Y, M050A, M050C, M050F, M050H, M050I, M050K, M050L, M050Q, M050R, M050S, M050T, M050V, M050W, M050Y, V051A, V051C, V051D, V051E, V051H, V051I, V051L, V051P, V051Q, P052C, P052D, P052E, P052F, P052H, P052I, P052K, P052L, P052Q, P052R, P052S, P052T, P052V, P052W, P052Y, S053E, S053F, S053G, S053H, S053I, S053K, S053L, S053M, S053N, S053Q, S053R, S053T, S053V, S053W, E054A, E054N, E054Q, E054S, T055A, T055C, T055D, T055F, T055G, T055H, T055I, T055K, T055M, T055P, T055Q, T055R, T055S, T055V, T055W, T055Y, N056D, N056M, N056P, N056Q, N056S, N056T, N056V, P057N, P057Q, P057T, P057V, P057W, F058C, F058E, F058G, F058H, F058L, F058M, F058N, F058Q, F058S, F058V, F058Y, Q059A, Q059C, Q059D, Q059E, Q059F, Q059G, Q059H, Q059K, Q059L, Q059M, Q059N, Q059P, Q059R, Q059S, Q059T, Q059V, Q059W, Q059Y, D060E, D060G, N062A, N062C, N062D, N062E, N062F, N062G, N062H, N062I, N062K, N062L, N062M, N062Q, N062R, N062S, N062T, N062V, N062W, N062Y, T066S, T066W, T066Y, H067A, H067C, H067F, H067I, H067L, H067M, H067N, H067P, H067R, H067S, H067T, T071I, T071Y, N077S, S078A, S078C, S078D, S078F, S078G, S078I, S078K, S078L, S078M, S078N, S078P, S078Q, S078R, S078T, S078V, S078W, S078Y, I079A, I079C, I079E, I079F, I079G, I079H, I079K, I079L, I079N, I079Q, I079R, I079S, I079T, I079V, I079W, I079Y, V081F, V081I, V081L, V081M, V081T, G083F, G083P, Q084A, Q084C, Q084H, Q084I, Q084N, Q084T, A085C, A085F, A085G, A085R, A085S, P086A, P086D, P086E, P086G, P086M, P086N, P086Q, P086R, P086S, P086T, P086W, P086Y, S089C, S089D, S089E, S089F, S089G, S089H, S089K, S089L, S089V, S089W, S089Y, L090A, L090D, L090E, L090G, L090H, L090M, L090Q, L090T, L090V, Y091A, Y091C, Y091D, Y091E, Y091F, Y091H, Y091I, Y091L, Y091M, Y091Q, Y091S, Y091T, Y091V, L096F, L096H, L096I, L096K, L096M, L096T, L096V, G097A, G097C, G097D, G097E, G097H, G097K, G097L, G097M, G097P, G097Q, G097R, G097S, G097T, G097V, A098C, A098D, A098F, A098G, A098H, A098I, A098L, A098P, A098Q, A098R, A098S, A098T, A098V, A098Y, D099C, D099E, D099I, D099K, D099L, D099N, D099P, D099Q, D099R, D099S, D099T, S101A, S101C, S101E, S101F, S101G, S101I, S101K, S101L, S101M, S101N, S101P, S101Q, S101R, S101T, S101V, S101Y, G102A, G102C, G102E, G102F, G102I, G102N, G102S, G102V, G102Y, Q103A, Q103C, Q103E, Q103F, Q103G, Q103I, Q103K, Q103L, Q103M, Q103N, Q103R, Q103S, Q103T, Q103V, Q103W, S105A, S105C, S105D, S105E, S105F, S105G, S105I, S105K, S105L, S105M, S105N, S105P, S105R, S105V, S105W, W106A, W106C, W106E, W106F, W106G, W106H, W106I, W106L, W106M, W106N, W106R, W106S, W106T, W106V, W106Y, N109A, N109C, N109E, N109F, N109G, N109H, N109L, N109M, N109P, N109Q, N109R, N109S, N109T, N109V, N109W, N109Y, I111C, I111F, I111L, I111M, I111N, I111P, I111T, I111V, I111W, E112A, E112C, E112D, E112F, E112G, E112I, E112L, E112M, E112N, E112Q, E112R, E112S, E112T, E112V, E112W, E112Y, W113D, W113E, W113F, W113N, W113P, W113Q, W113S, W113V, W113Y, I115E, I115H, I115N, I115R, I115T, I115V, I115W, I115Y, A116C, A116D, A116E, A116F, A116G, A116H, A116I, A116K, A116L, A116M, A116N, A116P, A116Q, A116R, A116S, A116T, A116V, A116W, A116Y, N118A, N118C, N118D, N118E, N118F, N118G, N118H, N118I, N118K, N118L, N118M, N118Q, N118R, N118S, N118T, N118V, N118W, N118Y, I122A, I122C, I122H, I122K, I122L, I122M, I122N, I122P, N123A, N123C, N123D, N123E, N123G, N123I, N123L, N123M, N123Q, N123S, N123T, N123V, M124C, M124D, M124I, M124L, M124S, M124T, M124V, M124W, S125A, S125C, S125E, S125F, S125I, S125K, S125M, S125N, S125P, S125Q, S125R, S125T, S125W, L126A, L126C, L126I, L126K, L126N, L126R, L126S, L126T, L126V, L126W, L126Y, G127A, G127C, G127E, G127F, G127I, G127K, G127M, G127N, G127P, G127Q, G127S, G127T, G127V, G127W, G127Y, G128A, G128D, G128F, G128H, G128L, G128N, G128P, G128S, G128T, G128V, G128W, G128Y, P129A, P129C, P129D, P129E, P129F, P129G, P129I, P129K, P129L, P129M, P129N, P129Q, P129S, P129T, P129V, P129Y, G131A, G131C, G131E, G131F, G131K, G131L, G131M, G131N, G131P, G131Q, G131R, G131S, G131T, G131V, G131W, G131Y, A133C, A133D, A133E, A133F, A133G, A133I, A133K, A133L, A133M, A133P, A133R, A133S, A133T, A133V, A133W, A133Y, A134D, A134E, A134F, A134G, A134I, A134K, A134L, A134M, A134P, A134Q, A134R, A134S, A134T, A134V, A134W, L135D, L135E, L135M, L135R, L135W, L135Y, K136E, K136H, K136L, K136M, K136N, K136R, K136S, K136T, K136V, K136W, K136Y, A137C, A137E, A137F, A137H, A137K, A137L, A137M, A137N, A137P, A137Q, A137R, A137S, A137T, A137V, A137W, A137Y, V139C, V139I, V139L, V139N, V139S, V139T, K141A, K141C, K141D, K141E, K141F, K141G, K141H, K141I, K141L, K141M, K141N, K141Q, K141R, K141S, K141V, K141W, K141Y, V143A, V143C, V143D, V143E, V143F, V143G, V143K, V143L, V143M, V143N, V143Q, V143R, V143S, V143T, V143W, A144C, A144D, A144E, A144G, A144I, A144K, A144L, A144M, A144R, A144S, A144T, A144V, A144W, S145A, S145C, S145D, S145E, S145F, S145G, S145H, S145I, S145L, S145M, S145Q, S145R, S145T, S145V, S145W, S145Y, G146A, G146C, G146D, G146E, G146M, G146Q, G146R, G146S, G146T, G146Y, A153S, G154L, G154P, G154T, E156A, E156C, E156F, E156K, E156L, E156N, E156Q, E156R, E156S, E156T, E156V, E156W, E156Y, T158A, T158D, T158E, T158G, T158H, T158I, T158K, T158L, T158M, T158N, T158Q, T158S, T158V, T158Y, S159A, S159C, S159D, S159E, S159G, S159H, S159I, S159K, S159M, S159Q, S159R, S159T, G160D, G160E, G160K, G160N, G160P, G160Q, G160S, G160T, S162A, S162C, S162E, S162H, S162K, S162L, S162M, S162N, S162Q, S162R, S162T, S162V, S163G, S163P, Y167A, Y167F, Y167H, Y167I, P168D, P168G, P168I, P168M, P168S, P168Y, G169A, G169E, G169F, G169H, G169I, G169M, G169N, G169R, G169T, G169V, G169Y, K170A, K170C, K170F, K170G, K170H, K170R, K170V, K170W, K170Y, Y171G, Y171K, Y171P, P172A, P172C, P172E, P172K, P172L, P172M, P172N, P172Q, P172R, P172S, P172T, P172V, P172Y, S173A, S173C, S173E, S173I, S173T, S173V, V174C, V174F, V174H, V174R, V174T, I175G, I175L, I175M, I175R, I175T, I175V, A176C, A176E, A176F, A176K, A176M, A176S, A176Y, A179G, V180A, V180C, V180L, V180N, V180S, V180T, D181C, D181E, D181G, D181H, D181M, D181N, D181S, D181T, D181W, S182A, S182C, S182D, S182F, S182G, S182H, S182I, S182K, S182M, S182P, S182Q, S182R, S182V, S182Y, S183A, S183C, S183E, S183F, S183G, S183H, S183I, S183K, S183L, S183M, S183N, S183Q, S183R, S183T, S183V, S183W, S183Y, N184C, N184D, N184E, N184G, N184H, N184K, N184L, N184M, N184Q, N184S, N184T, N184V, N184W, Q185A, Q185C, Q185E, Q185F, Q185G, Q185H, Q185I, Q185K, Q185L, Q185M, Q185N, Q185S, Q185T, Q185V, Q185W, R186I, R186L, R186W, A187C, A187D, A187E, A187F, A187G, A187P, A187S, A187W, A187Y, S188A, S188C, S188D, S188E, S188F, S188G, S188H, S188I, S188K, S188L, S188M, S188P, S188Q, S188T, S188V, S188W, S188Y, S190F, S190H, S190I, S190K, S191A, S191G, S191N, S191P, V192A, V192S, V192T, V192Y, G193F, G193H, G193I, G193N, G193P, G193R, G193T, P194C, P194E, P194H, P194I, P194K, P194L, P194M, P194Q, P194T, P194V, P194W, L196A, M199P, M199S, A200C, A200G, A200K, A200Y, G202D, G202E, G202F, G202L, G202P, G202V, G202Y, Q206A, Q206C, Q206D, Q206E, Q206F, Q206G, Q206H, Q206I, Q206L, Q206M, Q206N, Q206P, Q206R, Q206S, Q206T, Q206V, Q206W, Q206Y, S207D, S207E, S207K, S207Q, S207T, S207V, P210A, P210C, P210S, P210T, N212A, N212C, N212E, N212F, N212G, N212H, N212K, N212L, N212M, N212P, N212Q, N212R, N212S, N212V, K213A, K213C, K213D, K213E, K213F, K213H, K213I, K213L, K213M, K213N, K213Q, K213R, K213S, K213T, K213V, K213Y, Y214W, G215A, G215C, G215D, G215E, G215I, G215M, G215N, G215Q, G215S, G215T, G215V, A216C, A216D, A216E, A216G, A216K, A216L, A216M, A216N, A216P, A216Q, A216R, A216S, A216V, A216W, Y217A, Y217C, Y217D, Y217E, Y217F, Y217G, Y217H, Y217I, Y217K, Y217L, Y217M, Y217N, Y217Q, Y217R, Y217S, Y217T, Y217V, Y217W, N218A, N218C, N218E, N218F, N218G, N218H, N218K, N218M, N218R, N218S, N218T, N218W, N218Y, G219A, G219C, G219D, G219H, G219I, G219M, G219P, G219Q, G219R, G219S, G219T, G219V, G219W, T220D, T220E, T220F, T220G, T220K, T220M, T220S, T220Y, A223E, A223F, A223L, A223M, A223R, A223S, A223V, A223W, A223Y, S224A, S224C, S224F, S224G, S224H, S224M, S224N, S224Q, S224R, S224T, P225A, P225C, P225F, P225G, P225H, P225I, P225K, P225L, P225M, P225R, P225S, P225T, P225V, P225Y, A228P, A228R, A228S, A228T, A228W, G229A, G229H, G229I, G229S, A230C, A230E, A230G, A230Q, A230R, A230S, A230T, A230V, A231C, A231I, A231P, A231R, I234A, I234C, I234L, I234M, I234N, I234P, I234Q, I234S, I234T, I234V, L235A, L235C, L235G, L235I, L235K, L235M, L235N, L235Q, L235R, L235S, L235T, L235V, L235W, L235Y, S236A, S236C, S236D, S236E, S236G, S236H, S236N, S236Q, S236T, S236V, S236Y, K237A, K237E, K237F, K237G, K237H, K237I, K237L, K237M, K237N, K237Q, K237R, K237S, K237T, K237V, K237W, K237Y, H238C, H238D, H238E, H238F, H238M, H238R, H238S, P239C, P239D, P239E, P239F, P239H, P239L, P239M, P239N, P239Q, P239R, P239S, P239T, P239V, P239W, P239Y, N240A, N240C, N240D, N240F, N240G, N240K, N240L, N240Q, N240R, N240S, N240T, N240V, N240W, N240Y, W241A, W241F, W241G, W241H, W241I, W241K, W241M, W241Q, W241T, W241V, T242A, T242C, T242E, T242F, T242G, T242K, T242M, T242N, T242P, T242R, T242S, T242W, T242Y, N243C, N243E, N243F, N243G, N243I, N243Q, N243S, N243T, N243V, N243W, N243Y, T244A, T244D, T244F, T244G, T244H, T244K, T244L, T244M, T244N, T244P, T244Q, T244R, T244S, T244V, T244W, T244Y, Q245A, Q245C, Q245D, Q245E, Q245H, Q245I, Q245K, Q245L, Q245M, Q245R, Q245T, Q245V, Q245Y, R247W, S248A, S248E, S248F, S248G, S248H, S248I, S248L, S248M, S248N, S248Q, S248R, S248T, S248V, S248W, S248Y, S249C, S249D, S249H, S249I, S249K, S249L, S249M, S249N, S249Q, S249R, S249T, S249V, S249W, S249Y, L250D, L250F, L250H, L250I, L250M, L250T, L250V, E251A, E251T, E251W, N252A, N252C, N252E, N252G, N252H, N252I, N252L, N252M, N252Q, N252R, N252S, N252T, N252V, N252Y, T253A, T253C, T253E, T253G, T253H, T253K, T253M, T253S, T253V, T254A, T254C, T254L, T254M, T254R, T254S, T254V, T255A, T255C, T255D, T255E, T255F, T255G, T255H, T255I, T255K, T255L, T255M, T255R, T255S, T255V, K256A, K256C, K256D, K256E, K256F, K256H, K256I, K256L, K256M, K256N, K256P, K256Q, K256R, K256S, K256T, K256V, K256W, K256Y, L257A, L257C, L257F, L257G, L257H, L257I, L257K, L257M, L257N, L257R, L257S, L257T, L257V, L257W, L257Y, G258Q, D259A, D259E, D259F, D259G, D259L, D259N, D259P, D259Q, D259R, D259S, D259T, D259V, D259W, D259Y, S260A, S260C, S260D, S260E, S260F, S260G, S260H, S260L, S260M, S260N, S260P, S260R, S260V, S260W, S260Y, F261H, F261W, Y262A, Y262C, Y262E, Y262F, Y262H, Y262L, Y262M, Y262N, Y263F, Y263M, Y263T, G264F, G264I, G264L, K265A, K265C, K265E, K265G, K265H, K265L, K265M, K265N, K265Q, K265R, K265S, K265W, K265Y, G266C, G266F, G266L, G266M, G266P, G266R, G266V, G266W, G266Y, L267A, L267C, L267E, L267G, L267H, L267I, L267M, L267N, L267Q, L267S, L267T, L267V, I268A, I268C, I268K, I268L, I268M, I268P, I268R, I268V, N269D, N269E, N269K, N269L, N269P, N269Q, N269S, Q271A, Q271C, Q271D, Q271E, Q271F, Q271G, Q271H, Q271I, Q271K, Q271L, Q271M, Q271N, Q271P, Q271R, Q271S, Q271T, Q271V, Q271W, Q271Y, A272E, A272F, A272G, A272H, A272K, A272L, A272M, A272N, A272Q, A272R, A272S, A272T, A272V, A272W, A272Y, A274C, A274D, A274F, A274G, A274H, A274I, A274K, A274L, A274Q, A274S, A274T, and A274V.

In some preferred embodiments, the substitution comprises a combination selected from: Y021H-A045V-Y217E, Y021W-S101E-G128R-Y217Q, Y021H-Y217E, Y021H-A045V-S101N-Y217Q, Y021H-A045I-Y217E, Y021H-A045I-S101E-Y217Q, Y021W-A045I-S101E-Y217E, D036N-S101E-Y217L, Y021H-A045V-Y217Q, Y021H-A045I-S101E-Y217L, Y021H-A045I-Y217E, Y021H-Y217Q, Y021W-S101E-Y217L, Y021W-A045V-S101E-Y217L, Y021H-A045V-S101E-Y217E, S101E-Y217L, Y021H-A045V-S101E-Y217Q, Y021H-Y217L, Y021W-A045I-S101N-Y217L, S101N-K213I-Y217Q, Y021W-S101N-Y217L, Y021H-S101E-Y217E, M119F-K213K-Y217Q, Y021W-A045V-Y217E, Y021W-A045I-Y217E, M119F-K213I-Y217Q, Y021W-Y217E-N212S, M119F-K213L-Y217E, K213I-Y217Q, A045I-Y217Q, Y021W-A045V-S101E-Y217Q, Y021H-A045V-S101E-Y217L, S101S-M119F-K213I-Y217Q, K213N-Y217Q, M119F-Y217Q, S024H-A092G-A114G, S101N-M119F-K213I-Y217Q, S101N-K213L-Y217Q, S101N-M119F-K213K-Y217L, S101N-M119F-K213I-Y217L, Y021H-A045V-S101E, S101N-K213L-Y217E, A045V-Y217L, S101N-K213I-Y217L, S101S-M119M-K213K-Y217L, Y021H-Y217L, S101E-K213L-Y217L, K213I-Y217E, S101N-M119F-Y217E, Y021W-A045V-Y217L, A092G-A114G, S024H-A092G-Q103E, Y021W-S101E, V26Q-K213I, Y021H-S101N, S101E-K213N-Y217E. In some embodiments, the substitution comprises a combination selected from: S024S-V028V-M050M-A092A-Q103E-A114G-V246V, S024S-V028V-M050V-A092A-Q103Q-A114A-V246V, S024S-V028V-M050V-A092A-Q103Q-A114G-V246V, S024H-V028V-M050V-A092A-Q103Q-A114A-V246T, S024H-V028V-M050V-A092A-Q103E-A114A-V246V, S024H-V028V-M050V-A092A-Q103Q-A114G-V246V, S024H-V028V-M050M-A092A-Q103E-A114A-V246V, S024H-V028V-M050M-A092A-Q103E-A114A-V246T, S024S-V028V-M050M-A092G-Q103Q-A114A-V246T, S024H-V028V-M050M-A092A-Q103Q-A114G-V246T, S101E-M119N-K213N, S101N-K213I, S101N-M119H, M119H-K213I-Y217L, S101N-M119H-K213N-Y217L, S101N-K213L-Y217E, M119N-K213N-Y217L, M119F-K213L-Y217E, S101P-K213N, S101N-M119H-K213N, S101N-M119F-K213I-Y217L, K213L, M119N-K213N, K213N, K213I-Y217E, S101N-M119H-Y217Q, S101P-K213N-Y217L, M119N-K213I, K213N-Y217Q, M119H-K213N, S101N-K213L-Y217Q, S101P-K213N, S101E-K213N-Y217E, S101E-M119H-K213I-Y217Q, S101E-M119H-K213N, K213I-Y217Q, S101N-K213I-Y217Q, M119H-Y217Q, S101N-M119N-K213N-Y217Q, M119H-K213I-Y217Q, K213I-Y217Q, S101E-M119N-Y217L, M119F-K213L, M119H-K213N-Y217E, S101N-M119N-K213N-Y217Q, S101N-M119H-K213N-Y217Q, M119H-K213I-Y217Q, Y217Q, M119H-K213N-Y217Q, S101N-M119F-Y217E, M119F-Y217Q, S101N-M119F-K213I-Y217Q, S101N-K213I-Y217L, S101N-M119H-K213N-Y217L, S101E-K213L-Y217L, S101N-K213N-Y217Q, S101N-M119H-K213L, S101N-M119H-K213I, S101P-K213N-Y217L, M119F-K213I-Y217Q, S101N-K213I-Y217Q, S101E-M119H-K213I-Y217L, S101N-M119H-K213I-Y217Q, M119H-K213N-Y217E, S101N-M119N-K213N-Y217L, A048E-K213L, A048H-K213L, V026Q-A048Y-K213L, K213N, V026N-K213L, V026N-K213L, V026Y-K213N, A048D-K213N, V026Q-A048E-K213L, A048H-K213N, V026Q-A048H-K213L, A048H-K213L, K213L, K213N, V147D-K213L, K213I, V026Q-A048E-K213N, V026N-A048E-K213N, A048E-K213L, V026Y-A048E-K213I, A048D-K213N, K213I, A048H-K213N, V147D-K213N, Y021H-A045V-S101E-Y217L, Y021H-Y217L, Y021H-A045V-S101E-Y217Q, Y021H-A045I-S101E-Y217L, Y021H-Y217Q, Y021H-A045V-Y217E, A045V-Y217L, Y021H-A045V-S101N-Y217Q, Y021W-S101P-Y217L, Y021W-A045I-Y217E, Y021H-A045V-S101E-Y217E, Y021H-A045I-S101E-Y217L, Y021H-A045I-S101E-Y217Q, Y021H-A045V-Y217E, Y021W-S101E-Y217L, S101E-Y217L, Y021H-A045V-Y217Q, Y021H-Y217E, Y021W-Y217E-(N0212S), A045I-Y217Q, Y021H-A045V-Y217E, Y021W-A045V-S101E-Y217Q, Y021H-S101E-Y217E, Y021W-S101N-Y217L, S024S-V028V-M050M-A092A-Q103Q-A114A-V246T, Y021H-A045V-S101E, Y021W-A045V-S101E-Y217L, S101N-M119H-K213K-Y217Q, S101S-M119N-K213N-Y217Q, Y021H-A045V-S101P-Y217L, S024S-V028V-M050M-A092A-Q103Q-A114G-V246T, S101S-M119F-K213I-Y217Q, S101S-M119M-K213K-Y217L, Y021H-A045I-S101E-Y217Q, Y021H-A045V-S101E-Y217E, Y021H-A045V-S101E, Y021H-Y217L, Y021H-A045I-Y217E, Y021W-A045I-S101E-Y217E, S101N-M119F-K213K-Y217L, S101E-M119H-K213N-Y217E, Y021H-A045I-Y217E, S101S-M119H-K213L-Y217L, Y021H-Y217E, S101S-M119F-K213K-Y217Q, and Y021H-A045I-S101E-Y217L. In some embodiments, the substitution comprises a combination selected from: S024S-V028T-M050V-A092G-Q103E-A114G-V246T, S101N-M119H, M119N-K213N-Y217L, Y217L, M119N-K213N, K213N, K213N-Y217Q, S101E-K213N-Y217E, S101E-M119N-Y217L, Y217Q, S101N-M119N-K213N-Y217E, S101N-M119N-K213N-Y217L, Y021H-A045I-S101E-Y217L, S101E-Y217L, A045I-Y217Q, S101S-M119M-K213K-Y217L, Y021H-A045I-S101E-Y217L.

The present invention further provides the variants set forth in the Tables included in the Examples, as well as compositions comprising these variants.

Also provided by the present invention are isolated nucleic acids encoding the subtilisin variant, expression vectors comprising the nucleic acids, and host cells comprising the expression vector. Moreover the present invention provides cleaning compositions comprising the subtilisin variant. In some embodiments, the cleaning composition is a laundry detergent. In some embodiments, the laundry detergent is a cold water detergent, a low pH detergent, or a compact detergent. Moreover the present invention provides methods for producing a subtilisin variant of a Bacillus subtilisin, comprising: transforming a host cell with an expression vector comprising a nucleic acid encoding the subtilisin variant; and cultivating the transformed host cell under conditions suitable for the production of the subtilisin variant. In some embodiments, the methods further comprise the step of harvesting the produced subtilisin variant. In some embodiments, the host cell is a Bacillus species, and in a subset of these embodiments, the Bacillus species is B. subtilis. Moreover the present invention provides a method of cleaning, comprising the step of contacting a surface and/or an article comprising a fabric with a cleaning composition comprising an isolated subtilisin variant.

Additionally the present invention provides methods for protease engineering comprising the steps of: a) providing a plurality of site evaluation libraries (SELs) each comprising a plurality of protease variants having distinct substitutions at an identical amino acid position of the protease; b) testing the protease variants of the SELs and a standard protease in a test of a property of interest; c) determining a performance index (PI) for each of the protease variants for the test; d) identifying two or more of the amino acid positions as non-restrictive positions, wherein at least one of the plurality of protease variants in each of two of the SELs has a PI greater than 0.5; and f) providing a multiple mutation library comprising a plurality of multiply-substituted protease variants each comprising substitutions in the two or more non-restrictive positions. In some embodiments, the test comprises two or more different assays selected from the group consisting of stain removal assays (microswatch), LAS stability assays, detergent stability assays, and specific activity assays. In some embodiments the protease is selected from the group consisting of a bacterial serine protease, a bacterial subtilisin, and a bacterial neutral metalloprotease.

In further embodiments, the present invention provides methods for producing a multiply substituted subtilisin variant of a Bacillus subtilisin, comprising: testing a plurality of singly-substituted subtilisin variants in a first test of a first property and a second test of a second property, wherein the property of a parent subtilisin is given a value of 1.0 in each test, a favorable first or second property has a value greater than 1.0, and an unduly unfavorable first or second property has a value less than about 0.80 or in some preferred embodiments, less than about 0.60; identifying a substitution in at least one of the singly-substituted subtilisin variants that is associated with a favorable first property and which is not associated with an unduly unfavorable second property; identifying a substitution in at least one of the singly-substituted subtilisin variants that is associated with a favorable second property and which is not associated with an unduly unfavorable first property; and introducing the substitution from the previous steps into a subtilisin to yield a multiply-substituted subtilisin variant. In some embodiments, the methods further comprise testing the multiply-substituted subtilisin variant in the first test and the second test, wherein an improved subtilisin variant achieves a value of greater than 1.0 in both of the first and second tests, or a value of greater than 1.0 in the first test and a value of 0.80 to 1.0 in the second test. In some embodiments, the methods further comprise producing the improved subtilisin variant(s). In some embodiments, the first and second properties are negatively correlated. In some embodiments, a favorable first or second property has a value greater than about 1.2. In some embodiments, an unduly unfavorable first or second property has a value less than about 0.40. In some embodiments, the first property is stability, and the second property is wash performance. In a subset of these the stability comprises stability in detergent and wash performance comprises blood milk ink (BMI) wash performance in detergent. In some embodiments, the parent bacterial subtilisin is a wild type mature form of a B. amyloliquefaciens subtilisin BPN′ having an amino acid sequence set forth as SEQ ID NO:2. In other embodiments, the parent bacterial subtilisin is a wild type of a B. lentus GG36 subtilisin having an amino acid sequence set forth as SEQ ID NO:562, or a BPN″ comprising a Y217L substitution (SEQ ID NO:565), alone or in combination with other modifications. In some embodiments of the present invention, wash performance is tested in a powder or liquid detergent composition having a pH of between 5 and 12.0. It is not intended that the steps be limited to the exact order listed above, as any suitable order finds use in the present invention. However in some preferred embodiments, the substitutions are in positions in a parent subtilisin having a solvent accessible surface (SAS) of greater than about 50% or greater than about 65%.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A provides a map of pHPLT-VAAc1, while FIG. 1B provides a map of pHPLT-BPN′.

FIG. 2A depicts BMI cleaning performance of a BPN′-Y217L CCL in North American laundry detergent as a function of charge change. Similarly FIG. 2B depicts BMI cleaning performance of a GG36 CCL in North American laundry detergent as a function of charge change.

FIG. 3A depicts BMI cleaning performance of a BPN′-Y217L CCL in Western European liquid laundry detergent as a function of charge change. Similarly FIG. 3B depicts BMI cleaning performance of a GG36 CCL in Western European liquid laundry detergent as a function of charge change.

FIG. 4A depicts BMI cleaning performance of a BPN′-Y217L CCL in Japanese powdered laundry detergent as a function of charge change. Similarly FIG. 4B depicts BMI cleaning performance of a GG36 CCL in Japanese powdered laundry detergent as a function of charge change.

FIG. 5A depicts baked egg yolk cleaning performance of a BPN′-Y217L CCL in automatic dish washing detergent as a function of charge change. Similarly FIG. 5B depicts baked egg yolk cleaning performance of a GG36 CCL in automatic dish washing detergent as a function of charge change.

FIG. 6 depicts LAS/EDTA stability as a function of net charge change relative to parent BPN′-Y217L, for a library containing 80 variants.

DESCRIPTION OF THE INVENTION

The present invention provides methods for protein engineering. Specifically, the invention provides methods utilizing site evaluation libraries.

For practical purposes, it is not usually necessary to find the best sequence in a protein space in order to create a protein that is optimum for a particular application. For most applications, the problem to be solved is to identify at least one protein sequence that meets or exceeds the minimum value required for a number of properties. This requires knowledge of mutations that are good for a particular property, as well as knowledge of those mutations that are bad for any of the desired properties. The present invention provides means to meet the goal by identifying those positions in the protein that can be altered to improve the primary property and keep the values for other properties within desired limits.

The present invention provides means to evaluate all positions in a protein for all the properties of interest by building “site evaluation libraries” at each site. In preferred embodiments, these libraries contain 9-19 mutations at each position, and are used to evaluate each position for use in engineering the protein and constructing libraries. Each property is measured relative to the parent enzyme and an apparent free energy difference for each mutant vs. wild type is calculated. These delta delta G (“i.e., ΔΔG”) apparent values are then used to determine additivity.

An ideal way to analyze variants would be through the difference in free energy for the variant versus the parent protein in the process of interest. The Gibbs Free Energy for a process represents the maximum amount of work that can be performed by a system. The change in Free energy relative to the parent enzyme (ΔΔG) is given as follows;

ΔG=−RT ln (k _(variant) /k _(parent))

where k_(varient) is the rate constant for the variant enzyme, and k_(parent) is the rate constant for the parent enzyme, R is the Gas law constant and T is the absolute temperature. Most assays are not constructed to allow determination of true Free Energies, so we utilized a quantity

ΔG _(app) =−RT ln (P _(variant) /P _(parent))

where P_(variant) is the performance value for the variant and P_(parent) is the performance value for the parent enzyme under the same conditions. The ΔΔG_(app) values may be expected to behave in a similar fashion as to ΔΔG for data distributions and additivity. However, since ΔΔG is the maximum amount of work that can be carried out by the variant compared to the parent enzyme, the quantity ΔΔG_(app) will generally underestimate the ΔΔG and lead to results that appear synergistic in that the properties of two additive positions may be greater than the value predicted by adding their ΔΔG_(app) values together.

The methods of the present invention used to design efficient libraries that were used to engineer multiple properties in parallel. Although certain enzymes are described herein, the methods apply to any protein of interest for engineering. Site evaluation libraries (SELs) were built as described herein by introducing from 12 to 19 substitutions at each of the positions. The resulting mutations were analyzed using activity and stability assays. The wild type amino acid is listed as a reference point for every position. For each property, measurements were used to determine the mean and standard deviation of ΔΔG_(app) for the parent enzyme. The parent mean (σ_(parent)) was normalized to 0, and the standard deviation (σ_(parent)) for ΔΔG_(app) was determined These values were used as the reference for each property at each position of the molecule. The site evaluation data were tested for evidence of correlation between properties. The ΔΔG_(app) values for each property were plotted versus each other property and correlation coefficients were calculated. The two activity measurements on protein substrates were correlated.

In order to analyze the positions within the amino acid sequence, two types of sites were defined. “Unproductive” sites have no mutant that is better than the parent enzyme, while “Productive” sites have at least one substitution that is better than the parent enzyme. The probability that a site will be Productive is given by the number of Productive sites divided by the total number of sites. Although the probability that any mutation will be better than the parent enzyme is low (i.e., 6%-28%) the probability that a given site will have at least one Up mutation is quite high.

It was of interest to determine how the Productive and Unproductive sites were distributed with respect to structural features (e.g., buried amino acids, interacting amino acids, positions near the active site, etc.) in the protease, as well as sequence sites that are conserved or changeable in evolution. To make this determination, the structure is examined and the sequence aligned with non-redundant homologs.

As indicated in the Examples, deleterious mutations for any property are correlated with deleterious mutations for every other property, regardless of correlations of the properties. Only a small number of positions (5-10%) have mutations that are bad for all properties. These positions define the “fold” and are conserved in evolution. The implication of this is that although identification of beneficial mutations for any property requires a truly predictive screen for that property, identification of mutations likely to be deleterious for any property can be accomplished using ANY screen. A simplified protein engineering strategy is to build SELs and screen using a simple activity and/or stability screen. The deleterious mutations are identified and those positions that have few deleterious mutations are used to build libraries and combinatorial mutations to improve multiple properties. Also, picking sites that are on the surface of the protein, have few interactions and are variable in sequence alignments provides a high proportion of productive sites. Sites that are on the interior of the molecule, have many contacts and are strongly conserved in evolution will have a high probability of having deleterious mutations and should be avoided. It is contemplated that any suitable method for analyzing sequence and/or structural information will find use in the present invention, including but not limited to computer and/or electronic methods and/or programs.

The methods provide pairwise comparisons of the numbers of variants with more than 5% wt activity and less than 5% activity for each of two properties, along with correlation coefficients for the two properties.

Library Design

In some particularly preferred embodiments, the site evaluation library data are used for combinatorial library design. Traditional directed evolution builds random libraries and screens large numbers of library for single properties, combines these and repeats the process. As several investigators have found (See e.g., Bloom et al., Curr. Opin. Struct. Biol., 15:447-452 [2005]; Bloom et al., Proc. Natl. Acad. Sci. USA 103:5869-5874 [2006]; and Guo et al., Proc. Natl. Acad. Sci. USA 101:9205-9210 [2004]), the accumulation of positive mutations for one property commonly leads to decreases in other properties. The probability that any mutation will be Up for any property is small, and the probability that any mutation will be Down is high (>85%), and the probability that accumulating more than three (3) mutations that increase activity will result in a decrease in several other properties is quite high. This problem is avoided by using the site evaluation data to build libraries that would be good for multiple properties. Unproductive sites were not included in combinatorial libraries, and productive sites were further classified by the percentage of mutations that were up.

Cleaning Compositions

The cleaning composition of the present invention are advantageously employed for example, in laundry applications, hard surface cleaning, automatic dishwashing applications, as well as cosmetic applications such as dentures, teeth, hair and skin. However, due to the unique advantages of increased effectiveness in lower temperature solutions, the enzymes of the present invention are ideally suited for laundry applications. Furthermore, the enzymes of the present invention may be employed in both granular and liquid compositions.

The variant proteases of the present invention also find use cleaning additive products. In some embodiments, low temperature solution cleaning applications find use. The additive product may be, in its simplest form, one or more proteases. In some embodiments, the additive is packaged in dosage form for addition to a cleaning process. Any suitable single dosage form also finds use with the present invention, including but not limited to pills, tablets, gelcaps, or other single dosage units such as pre-measured powders or liquids. In some embodiments, filler(s) or carrier material(s) are included to increase the volume of such composition. Suitable filler or carrier materials include, but are not limited to, various salts of sulfate, carbonate and silicate as well as talc, clay and the like. Suitable filler or carrier materials for liquid compositions include, but are not limited to water or low molecular weight primary and secondary alcohols including polyols and diols. Examples of such alcohols include, but are not limited to, methanol, ethanol, propanol and isopropanol. In some embodiments, the compositions contain from about 5% to about 90% of such materials. Acidic fillers find use to reduce pH. Alternatively, the cleaning additives include adjunct ingredients as more fully described below.

The present cleaning compositions and cleaning additives require an effective amount of at least one of the protease variants provided herein, alone or in combination with other proteases and/or additional enzymes. The required level of enzyme is achieved by the addition of one or more protease variants of the present invention. Typically the present cleaning compositions will comprise at least about 0.0001 weight percent, from about 0.0001 to about 1, from about 0.001 to about 0.5, or even from about 0.01 to about 0.1 weight percent of at least one of the variant proteases of the present invention.

The cleaning compositions herein are typically formulated such that, during use in aqueous cleaning operations, the wash water will have a pH of from about 5.0 to about 11.5 or even from about 7.5 to about 10.5. Liquid product formulations are typically formulated to have a neat pH from about 3.0 to about 9.0 or even from about 3 to about 5. Granular laundry products are typically formulated to have a pH from about 9 to about 11. Techniques for controlling pH at recommended usage levels include the use of buffers, alkalis, acids, etc., and are well known to those skilled in the art.

Suitable low pH cleaning compositions typically have a neat pH of from about 3 to about 5, and are typically free of surfactants that hydrolyze in such a pH environment. Such surfactants include sodium alkyl sulfate surfactants that comprise at least one ethylene oxide moiety or even from about 1 to about 16 moles of ethylene oxide. Such cleaning compositions typically comprise a sufficient amount of a pH modifier, such as sodium hydroxide, monoethanolamine or hydrochloric acid, to provide such cleaning composition with a neat pH of from about 3 to about 5. Such compositions typically comprise at least one acid stable enzyme. In some embodiments, the compositions are liquids, while in other embodiments, they are solids. The pH of such liquid compositions is typically measured as a neat pH. The pH of such solid compositions is measured as a 10% solids solution of said composition wherein the solvent is distilled water. In these embodiments, all pH measurements are taken at 20° C.

In some embodiments, when the variant protease(s) is/are employed in a granular composition or liquid, it is desirable for the variant protease to be in the form of an encapsulated particle to protect the variant protease from other components of the granular composition during storage. In addition, encapsulation is also a means of controlling the availability of the variant protease during the cleaning process. In some embodiments, encapsulation enhances the performance of the variant protease(s) and/or additional enzymes. In this regard, the variant proteases of the present invention are encapsulated with any suitable encapsulating material known in the art. In some embodiments, the encapsulating material typically encapsulates at least part of the catalyst for the variant protease(s) of the present invention. Typically, the encapsulating material is water-soluble and/or water-dispersible. In some embodiments, the encapsulating material has a glass transition temperature (Tg) of 0° C. or higher. Glass transition temperature is described in more detail in WO 97/11151. The encapsulating material is selected from consisting of carbohydrates, natural or synthetic gums, chitin, chitosan, cellulose and cellulose derivatives, silicates, phosphates, borates, polyvinyl alcohol, polyethylene glycol, paraffin waxes, and combinations thereof. When the encapsulating material is a carbohydrate, it is typically selected from monosaccharides, oligosaccharides, polysaccharides, and combinations thereof. Typically, the encapsulating material is a starch. Suitable starches are described in EP 0 922 499; U.S. Pat. No. 4,977,252; U.S. Pat. No. 5,354,559, and U.S. Pat. No. 5,935,826. In some embodiments, the encapsulating material is a microsphere made from plastic such as thermoplastics, acrylonitrile, methacrylonitrile, polyacrylonitrile, polymethacrylonitrile and mixtures thereof; commercially available microspheres that find use include those supplied by EXPANCEL® (Stockviksverken, Sweden), and PM 6545, PM 6550, PM 7220, PM 7228, EXTENDOSPHERES®, LUXSIL®, Q-CEL®, and SPHERICEL® (PQ Corp., Valley Forge, Pa.).

As described herein, the variant proteases of the present invention find particular use in the cleaning industry, including, but not limited to laundry and dish detergents. These applications place enzymes under various environmental stresses. The variant proteases of the present invention provide advantages over many currently used enzymes, due to their stability under various conditions.

Indeed, there are a variety of wash conditions including varying detergent formulations, wash water volumes, wash water temperatures, and lengths of wash time, to which proteases involved in washing are exposed. In addition, detergent formulations used in different geographical areas have different concentrations of their relevant components present in the wash water. For example, a European detergent typically has about 4500-5000 ppm of detergent components in the wash water, while a Japanese detergent typically has approximately 667 ppm of detergent components in the wash water. In North America, particularly the United States, detergents typically have about 975 ppm of detergent components present in the wash water.

A low detergent concentration system includes detergents where less than about 800 ppm of detergent components are present in the wash water. Japanese detergents are typically considered low detergent concentration system as they have approximately 667 ppm of detergent components present in the wash water.

A medium detergent concentration includes detergents where between about 800 ppm and about 2000 ppm of detergent components are present in the wash water. North American detergents are generally considered to be medium detergent concentration systems as they have approximately 975 ppm of detergent components present in the wash water. Brazil typically has approximately 1500 ppm of detergent components present in the wash water.

A high detergent concentration system includes detergents where greater than about 2000 ppm of detergent components are present in the wash water. European detergents are generally considered to be high detergent concentration systems as they have approximately 4500-5000 ppm of detergent components in the wash water.

Latin American detergents are generally high suds phosphate builder detergents and the range of detergents used in Latin America can fall in both the medium and high detergent concentrations as they range from 1500 ppm to 6000 ppm of detergent components in the wash water. As mentioned above, Brazil typically has approximately 1500 ppm of detergent components present in the wash water. However, other high suds phosphate builder detergent geographies, not limited to other Latin American countries, may have high detergent concentration systems up to about 6000 ppm of detergent components present in the wash water.

In light of the foregoing, it is evident that concentrations of detergent compositions in typical wash solutions throughout the world varies from less than about 800 ppm of detergent composition (“low detergent concentration geographies”), for example about 667 ppm in Japan, to between about 800 ppm to about 2000 ppm (“medium detergent concentration geographies”), for example about 975 ppm in U.S. and about 1500 ppm in Brazil, to greater than about 2000 ppm (“high detergent concentration geographies”), for example about 4500 ppm to about 5000 ppm in Europe and about 6000 ppm in high suds phosphate builder geographies.

The concentrations of the typical wash solutions are determined empirically. For example, in the U.S., a typical washing machine holds a volume of about 64.4 L of wash solution. Accordingly, in order to obtain a concentration of about 975 ppm of detergent within the wash solution about 62.79 g of detergent composition must be added to the 64.4 L of wash solution. This amount is the typical amount measured into the wash water by the consumer using the measuring cup provided with the detergent.

As a further example, different geographies use different wash temperatures. The temperature of the wash water in Japan is typically less than that used in Europe. For example, the temperature of the wash water in North America and Japan is typically between 10 and 30° C. (e.g., about 20° C.), whereas the temperature of wash water in Europe is typically between 30 and 60° C. (e.g., about 40° C.).

As a further example, different geographies typically have different water hardness. Water hardness is usually described in terms of the grains per gallon mixed Ca²⁺/Mg²⁺. Hardness is a measure of the amount of calcium (Ca²⁺) and magnesium (Mg²⁺) in the water. Most water in the United States is hard, but the degree of hardness varies. Moderately hard (60-120 ppm) to hard (121-181 ppm) water has 60 to 181 parts per million (parts per million converted to grains per U.S. gallon is ppm # divided by 17.1 equals grains per gallon) of hardness minerals.

Water Grains per gallon Parts per million Soft less than 1.0 less than 17 Slightly hard 1.0 to 3.5 17 to 60 Moderately hard 3.5 to 7.0 60 to 120 Hard 7.0 to 10.5 120 to 180 Very hard greater than 10.5 greater than 180

European water hardness is typically greater than 10.5 (for example 10.5-20.0) grains per gallon mixed Ca²⁺/Mg²⁺ (e.g., about 15 grains per gallon mixed Ca²⁺/Mg²⁺). North American water hardness is typically greater than Japanese water hardness, but less than European water hardness. For example, North American water hardness can be between 3 to 10 grains, 3-8 grains or about 6 grains. Japanese water hardness is typically lower than North American water hardness, usually less than 4, for example 3 grains per gallon mixed Ca²⁺/Mg²⁺.

Accordingly, in some embodiments, the present invention provides variant proteases that show surprising wash performance in at least one set of wash conditions (e.g., water temperature, water hardness, and/or detergent concentration). In some embodiments, the variant proteases of the present invention are comparable in wash performance to other subtilisin proteases. In some embodiments, the variant proteases of the present invention exhibit enhanced wash performance as compared to subtilisin proteases currently commercially available. Thus, in some preferred embodiments of the present invention, the variant proteases provided herein exhibit enhanced oxidative stability, enhanced thermal stability, and/or enhanced chelator stability. In addition, the variant proteases of the present invention find use in cleaning compositions that do not include detergents, again either alone or in combination with builders and stabilizers.

In some embodiments of the present invention, the cleaning compositions comprise at least one variant protease of the present invention at a level from about 0.00001% to about 10% by weight of the composition and the balance (e.g., about 99.999% to about 90.0%) comprising cleaning adjunct materials by weight of composition. In other aspects of the present invention, the cleaning compositions of the present invention comprises at least one variant protease at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% by weight of the composition and the balance of the cleaning composition (e.g., about 99.9999% to about 90.0%, about 99.999% to about 98%, about 99.995% to about 99.5% by weight) comprising cleaning adjunct materials.

In some embodiments, preferred cleaning compositions comprise one or more additional enzymes or enzyme derivatives which provide cleaning performance and/or fabric care benefits, in addition to one or more of the variant proteases provided herein. Such enzymes include, but are not limited to other proteases, lipases, cutinases, amylases, cellulases, peroxidases, oxidases (e.g. laccases), and/or mannanases.

Any other suitable protease finds use in the compositions of the present invention. Suitable proteases include those of animal, vegetable or microbial origin. In some particularly preferred embodiments, microbial proteases are used. In some embodiments, chemically or genetically modified mutants are included. In some embodiments, the protease is a serine protease, preferably an alkaline microbial protease or a trypsin-like protease. Examples of alkaline proteases include subtilisins, especially those derived from Bacillus (e.g., subtilisin, lentus, amyloliquefaciens, subtilisin Carlsberg, subtilisin 309, subtilisin 147 and subtilisin 168). Additional examples include those mutant proteases described in U.S. Pat. Nos. RE 34,606, 5,955,340, 5,700,676, 6,312,936, and 6,482,628, all of which are incorporated herein by reference. Additional protease examples include, but are not limited to trypsin (e.g., of porcine or bovine origin), and the Fusarium protease described in WO 89/06270. Preferred commercially available protease enzymes include MAXATASE®, MAXACAL™, MAXAPEM™, OPTICLEAN®, OPTIMASE®, PROPERASE®, PURAFECT® and PURAFECT® OXP (Genencor); ALCALASE®, SAVINASE®, PRIMASE®, DURAZYM™, RELASE® and ESPERASE® (Novozymes); and BLAP™ (Henkel Kommanditgesellschaft auf Aktien, Duesseldorf, Germany. Various proteases are described in WO95/23221, WO 92/21760, and U.S. Pat. Nos. 5,801,039, 5,340,735, 5,500,364, 5,855,625, U.S. Pat. No. RE 34,606, 5,955,340, 5,700,676, 6,312,936, and 6,482,628, and various other patents.

In addition, any suitable lipase finds use in the present invention. Suitable lipases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are encompassed by the present invention. Examples of useful lipases include Humicola lanuginosa lipase (See e.g., EP 258 068, and EP 305 216), Rhizomucor miehei lipase (See e.g., EP 238 023), Candida lipase, such as C. antarctica lipase (e.g., the C. antarctica lipase A or B; See e.g., EP 214 761), a Pseudomonas lipase such as P. alcaligenes and P. pseudoalcaligenes lipase (See e.g., EP 218 272), P. cepacia lipase (See e.g., EP 331 376), P. stutzeri lipase (See e.g., GB 1,372,034), P. fluorescens lipase, Bacillus lipase (e.g., B. subtilis lipase [Dartois et al., Biochem. Biophys. Acta 1131:253-260 [1993]); B. stearothermophilus lipase [See e.g., JP 64/744992]; and B. pumilus lipase [See e.g., WO 91/16422]).

Furthermore, a number of cloned lipases find use in some embodiments of the present invention, including but not limited to Penicillium camembertii lipase (See, Yamaguchi et al., Gene 103:61-67 [1991]), Geotricum candidum lipase (See, Schimada et al., J. Biochem., 106:383-388 [1989]), and various Rhizopus lipases such as R. delemar lipase (See, Hass et al., Gene 109:117-113 [1991]), a R. niveus lipase (Kugimiya et al., Biosci. Biotech. Biochem. 56:716-719 [1992]) and R. oryzae lipase.

Other types of lipolytic enzymes such as cutinases also find use in some embodiments of the present invention, including but not limited to the cutinase derived from Pseudomonas mendocina (See, WO 88/09367), and the cutinase derived from Fusarium solani pisi (See, WO 90/09446).

Additional suitable lipases include commercially available lipases such as M1 LIPASE™, LUMA FAST™, and LIPOMAX™ (Genencor); LIPOLASE® and LIPOLASE® ULTRA (Novozymes); and LIPASE P™ “Amano” (Amano Pharmaceutical Co. Ltd., Japan).

In some embodiments of the present invention, the cleaning compositions of the present invention further comprise lipases at a level from about 0.00001% to about 10% of additional lipase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In other aspects of the present invention, the cleaning compositions of the present invention also comprise, lipases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% lipase by weight of the composition.

Any amylase (alpha and/or beta) suitable for use in alkaline solutions also find use in some embodiments of the present invention. Suitable amylases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. Amylases that find use in the present invention, include, but are not limited to α-amylases obtained from B. licheniformis (See e.g., GB 1,296,839). Commercially available amylases that find use in the present invention include, but are not limited to DURAMYL®, TERMAMYL®, FUNGAMYL® and BAN™ (Novozymes) and RAPIDASE® and MAXAMYL® P (Genencor).

In some embodiments of the present invention, the cleaning compositions of the present invention further comprise amylases at a level from about 0.00001% to about 10% of additional amylase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In other aspects of the present invention, the cleaning compositions of the present invention also comprise, amylases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% amylase by weight of the composition.

In some further embodiments, any suitable cellulase finds used in the cleaning compositions of the present invention. Suitable cellulases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. Suitable cellulases include, but are not limited to Humicola insolens cellulases (See e.g., U.S. Pat. No. 4,435,307). Especially suitable cellulases are the cellulases having color care benefits (See e.g., EP 0 495 257). Commercially available cellulases that find use in the present include, but are not limited to CELLUZYME® (Novozymes), and KAC-500(B)™ (Kao Corporation). In some embodiments, cellulases are incorporated as portions or fragments of mature wild-type or variant cellulases, wherein a portion of the N-terminus is deleted (See e.g., U.S. Pat. No. 5,874,276). In some embodiments, the cleaning compositions of the present invention further comprise cellulases at a level from about 0.00001% to about 10% of additional cellulase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In other aspects of the present invention, the cleaning compositions of the present invention also comprise cellulases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% cellulase by weight of the composition.

Any mannanase suitable for use in detergent compositions also finds use in the present invention. Suitable mannanases include, but are not limited to those of bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. Various mannanases are known which find use in the present invention (See e.g., U.S. Pat. No. 6,566,114, U.S. Pat. No. 6,602,842, and U.S. Pat. No. 6,440,991, all of which are incorporated herein by reference). In some embodiments, the cleaning compositions of the present invention further comprise mannanases at a level from about 0.00001% to about 10% of additional mannanase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In other aspects of the present invention, the cleaning compositions of the present invention also comprise, mannanases at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% mannanase by weight of the composition.

In some embodiments, peroxidases are used in combination with hydrogen peroxide or a source thereof (e.g., a percarbonate, perborate or persulfate) in the compositions of the present invention. In some alternative embodiments, oxidases are used in combination with oxygen. Both types of enzymes are used for “solution bleaching” (i.e., to prevent transfer of a textile dye from a dyed fabric to another fabric when the fabrics are washed together in a wash liquor), preferably together with an enhancing agent (See e.g., WO 94/12621 and WO 95/01426). Suitable peroxidases/oxidases include, but are not limited to those of plant, bacterial or fungal origin. Chemically or genetically modified mutants are included in some embodiments. In some embodiments, the cleaning compositions of the present invention further comprise peroxidase and/or oxidase enzymes at a level from about 0.00001% to about 10% of additional peroxidase and/or oxidase by weight of the composition and the balance of cleaning adjunct materials by weight of composition. In other aspects of the present invention, the cleaning compositions of the present invention also comprise, peroxidase and/or oxidase enzymes at a level of about 0.0001% to about 10%, about 0.001% to about 5%, about 0.001% to about 2%, about 0.005% to about 0.5% peroxidase and/or oxidase enzymes by weight of the composition.

In some embodiments, additional enzymes find use, including but not limited to perhydrolases (See e.g., WO 05/056782). In addition, in some particularly preferred embodiments, mixtures of the above mentioned enzymes are encompassed herein, in particular one or more additional protease, amylase, lipase, mannanase, and/or at least one cellulase. Indeed, it is contemplated that various mixtures of these enzymes will find use in the present invention. It is also contemplated that the varying levels of the variant protease(s) and one or more additional enzymes may both independently range to about 10%, the balance of the cleaning composition being cleaning adjunct materials. The specific selection of cleaning adjunct materials are readily made by considering the surface, item, or fabric to be cleaned, and the desired form of the composition for the cleaning conditions during use (e.g., through the wash detergent use).

Examples of suitable cleaning adjunct materials include, but are not limited to, surfactants, builders, bleaches, bleach activators, bleach catalysts, other enzymes, enzyme stabilizing systems, chelants, optical brighteners, soil release polymers, dye transfer agents, dispersants, suds suppressors, dyes, perfumes, colorants, filler salts, hydrotropes, photoactivators, fluorescers, fabric conditioners, hydrolyzable surfactants, preservatives, anti-oxidants, anti-shrinkage agents, anti-wrinkle agents, germicides, fungicides, color speckles, silvercare, anti-tarnish and/or anti-corrosion agents, alkalinity sources, solubilizing agents, carriers, processing aids, pigments, and pH control agents (See e.g., U.S. Pat. Nos. 6,610,642, 6,605,458, 5,705,464, 5,710,115, 5,698,504, 5,695,679, 5,686,014 and 5,646,101, all of which are incorporated herein by reference). Embodiments of specific cleaning composition materials are exemplified in detail below. In embodiments in which the cleaning adjunct materials are not compatible with the variant proteases of the present invention in the cleaning compositions, then suitable methods of keeping the cleaning adjunct materials and the protease(s) separated (i.e., not in contact with each other) until combination of the two components is appropriate are used. Such separation methods include any suitable method known in the art (e.g., gelcaps, encapulation, tablets, physical separation, etc.).

In some preferred embodiments, an effective amount of one or more variant protease(s) provided herein are included in compositions useful for cleaning a variety of surfaces in need of proteinaceous stain removal. Such cleaning compositions include cleaning compositions for such applications as cleaning hard surfaces, fabrics, and dishes. Indeed, in some embodiments, the present invention provides fabric cleaning compositions, while in other embodiments, the present invention provides non-fabric cleaning compositions. Notably, the present invention also provides cleaning compositions suitable for personal care, including oral care (including dentrifices, toothpastes, mouthwashes, etc., as well as denture cleaning compositions), skin, and hair cleaning compositions. It is intended that the present invention encompass detergent compositions in any form (i.e., liquid, granular, bar, semi-solid, gels, emulsions, tablets, capsules, etc.).

By way of example, several cleaning compositions wherein the variant proteases of the present invention find use are described in greater detail below. In embodiments in which the cleaning compositions of the present invention are formulated as compositions suitable for use in laundry machine washing method(s), the compositions of the present invention preferably contain at least one surfactant and at least one builder compound, as well as one or more cleaning adjunct materials preferably selected from organic polymeric compounds, bleaching agents, additional enzymes, suds suppressors, dispersants, lime-soap dispersants, soil suspension and anti-redeposition agents and corrosion inhibitors. In some embodiments, laundry compositions also contain softening agents (i.e., as additional cleaning adjunct materials). The compositions of the present invention also find use detergent additive products in solid or liquid form. Such additive products are intended to supplement and/or boost the performance of conventional detergent compositions and can be added at any stage of the cleaning process. In some embodiments, the density of the laundry detergent compositions herein ranges from about 400 to about 1200 g/liter, while in other embodiments, it ranges from about 500 to about 950 g/liter of composition measured at 20° C.

In embodiments formulated as compositions for use in manual dishwashing methods, the compositions of the invention preferably contain at least one surfactant and preferably at least one additional cleaning adjunct material selected from organic polymeric compounds, suds enhancing agents, group II metal ions, solvents, hydrotropes and additional enzymes.

In some embodiments, various cleaning compositions such as those provided in U.S. Pat. No. 6,605,458 find use with the variant proteases of the present invention. Thus, in some embodiments, the compositions comprising at least one variant protease of the present invention is a compact granular fabric cleaning composition, while in other embodiments, the composition is a granular fabric cleaning composition useful in the laundering of colored fabrics, in further embodiments, the composition is a granular fabric cleaning composition which provides softening through the wash capacity, in additional embodiments, the composition is a heavy duty liquid fabric cleaning composition. In some embodiments, the compositions comprising at least one variant protease of the present invention are fabric cleaning compositions such as those described in U.S. Pat. Nos. 6,610,642 and 6,376,450. In addition, the variant proteases of the present invention find use in granular laundry detergent compositions of particular utility under European or Japanese washing conditions (See e.g., U.S. Pat. No. 6,610,642).

In some alternative embodiments, the present invention provides hard surface cleaning compositions comprising at least one variant protease provided herein. Thus, in some embodiments, the compositions comprising at least one variant protease of the present invention is a hard surface cleaning composition such as those described in U.S. Pat. Nos. 6,610,642, 6,376,450, and 6,376,450.

In yet further embodiments, the present invention provides dishwashing compositions comprising at least one variant protease provided herein. Thus, in some embodiments, the compositions comprising at least one variant protease of the present invention is a hard surface cleaning composition such as those in U.S. Pat. Nos. 6,610,642 and 6,376,450. In still further embodiments, the present invention provides dishwashing compositions comprising at least one variant protease provided herein. In some further embodiments, the compositions comprising at least one variant protease of the present invention comprise oral care compositions such as those in U.S. Pat. Nos. 6,376,450, and 6,376,450. The formulations and descriptions of the compounds and cleaning adjunct materials contained in the aforementioned U.S. Pat. Nos. 6,376,450, 6,605,458, 6,605,458, and 6,610,642, find use with the variant proteases provided herein.

The cleaning compositions of the present invention are formulated into any suitable form and prepared by any process chosen by the formulator, non-limiting examples of which are described in U.S. Pat. Nos. 5,879,584, 5,691,297, 5,574,005, 5,569,645, 5,565,422, 5,516,448, 5,489,392, and 5,486,303, all of which are incorporated herein by reference. When a low pH cleaning composition is desired, the pH of such composition is adjusted via the addition of a material such as monoethanolamine or an acidic material such as HCl.

While not essential for the purposes of the present invention, the non-limiting list of adjuncts illustrated hereinafter are suitable for use in the instant cleaning compositions. In some embodiments, these adjuncts are incorporated for example, to assist or enhance cleaning performance, for treatment of the substrate to be cleaned, or to modify the aesthetics of the cleaning composition as is the case with perfumes, colorants, dyes or the like. It is understood that such adjuncts are in addition to the variant proteases of the present invention. The precise nature of these additional components, and levels of incorporation thereof, will depend on the physical form of the composition and the nature of the cleaning operation for which it is to be used. Suitable adjunct materials include, but are not limited to, surfactants, builders, chelating agents, dye transfer inhibiting agents, deposition aids, dispersants, additional enzymes, and enzyme stabilizers, catalytic materials, bleach activators, bleach boosters, hydrogen peroxide, sources of hydrogen peroxide, preformed peracids, polymeric dispersing agents, clay soil removal/anti-redeposition agents, brighteners, suds suppressors, dyes, perfumes, structure elasticizing agents, fabric softeners, carriers, hydrotropes, processing aids and/or pigments. In addition to the disclosure below, suitable examples of such other adjuncts and levels of use are found in U.S. Pat. Nos. 5,576,282, 6,306,812, and 6,326,348, that are incorporated by reference. The aforementioned adjunct ingredients may constitute the balance of the cleaning compositions of the present invention.

In some embodiments, the cleaning compositions according to the present invention comprise a surfactant or surfactant system wherein the surfactant is selected from nonionic surfactants, anionic surfactants, cationic surfactants, ampholytic surfactants, zwitterionic surfactants, semi-polar nonionic surfactants and mixtures thereof.

In some additional embodiments, the cleaning compositions of the present invention comprise one or more detergent builders or builder systems. Builders include, but are not limited to, the alkali metal, ammonium and alkanolammonium salts of polyphosphates, alkali metal silicates, alkaline earth and alkali metal carbonates, aluminosilicate builders polycarboxylate compounds. ether hydroxypolycarboxylates, copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1,3,5-trihydroxy benzene-2,4,6-trisulphonic acid, and carboxymethyloxysuccinic acid, the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid, as well as polycarboxylates such as mellitic acid, succinic acid, citric acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, carboxymethyloxysuccinic acid, and soluble salts thereof.

In some further embodiments, the cleaning compositions herein contain a chelating agent. Suitable chelating agents include copper, iron and/or manganese chelating agents and mixtures thereof.

In some still further embodiments, the cleaning compositions provided herein contain a deposition aid. Suitable deposition aids include, polyethylene glycol, polypropylene glycol, polycarboxylate, soil release polymers such as polytelephthalic acid, clays such as Kaolinite, montmorillonite, atapulgite, illite, bentonite, halloysite, and mixtures thereof.

In some additional embodiments, the cleaning compositions of the present invention also include one or more dye transfer inhibiting agents. Suitable polymeric dye transfer inhibiting agents include, but are not limited to, polyvinylpyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof.

In some still additional embodiments, the cleaning compositions of the present invention also contain dispersants. Suitable water-soluble organic materials include the homo- or co-polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms.

In some particularly preferred embodiments, the cleaning compositions comprise one or more detergent enzymes which provide cleaning performance and/or fabric care benefits. Examples of suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, phospholipases, esterases, cutinases, pectinases, keratinases, reductases, oxidases, phenol oxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, β-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, and amylases, or mixtures thereof. A typical combination is cocktail of conventional applicable enzymes including at least one protease, at least one lipase, at least one cutinase, and/or at least one cellulase in conjunction with at least one amylase.

In some further embodiments, the enzymes used in the cleaning compositions are stabilized any suitable technique. In some embodiments, the enzymes employed herein are stabilized by the presence of water-soluble sources of calcium and/or magnesium ions in the finished compositions that provide such ions to the enzymes.

In some still further embodiments, the cleaning compositions of the present invention include catalytic metal complexes. One type of metal-containing bleach catalyst is a catalyst system comprising a transition metal cation of defined bleach catalytic activity, such as copper, iron, titanium, ruthenium, tungsten, molybdenum, or manganese cations, an auxiliary metal cation having little or no bleach catalytic activity, such as zinc or aluminum cations, and a sequestrate having defined stability constants for the catalytic and auxiliary metal cations, particularly ethylenediaminetetraacetic acid, ethylenediaminetetra (methylenephosphonic acid) and water-soluble salts thereof. Such catalysts are disclosed in U.S. Pat. No. 4,430,243.

In some embodiments, the compositions herein are catalyzed by means of a manganese compound. Such compounds and levels of use are well known in the art and include, for example, the manganese-based catalysts disclosed in U.S. Pat. No. 5,576,282. In addition, cobalt bleach catalysts useful herein are known, and are described, for example, in U.S. Pat. Nos. 5,597,936, and 5,595,967. Such cobalt catalysts are readily prepared by known procedures, such as taught for example in U.S. Pat. Nos. 5,597,936, and 5,595,967. In some embodiments, the compositions provided herein also suitably include a transition metal complex of a macropolycyclic rigid ligand (i.e., “MRL”). As a practical matter, and not by way of limitation, the compositions and cleaning processes herein are adjustable, to provide on the order of at least one part per hundred million of the active MRL species in the aqueous washing medium, and will preferably provide from about 0.005 ppm to about 25 ppm, more preferably from about 0.05 ppm to about 10 ppm, and most preferably from about 0.1 ppm to about 5 ppm, of the MRL in the wash liquor. Preferred transition-metals in the instant transition-metal bleach catalyst include manganese, iron and chromium. Preferred MRLs herein are a special type of ultra-rigid ligand that is cross-bridged such as 5,12-diethyl-1,5,8,12-tetraazabicyclo[6.6.2]hexadecane. Suitable transition metal MRLs are readily prepared by known procedures, such as taught for example in WO 00/332601, and U.S. Pat. No. 6,225,464.

As indicated above, the cleaning compositions of the present invention are formulated into any suitable form and prepared by any process chosen by the formulator, non-limiting examples of which are described in U.S. Pat. Nos. 5,879,584, 5,691,297, 5,574,005, 5,569,645, 5,516,448, 5,489,392, and 5,486,303, all of which are incorporated herein by reference.

The cleaning compositions disclosed herein of find use in cleaning a situs (e.g., a surface, dishware, or fabric). Typically, at least a portion of the situs is contacted with an embodiment of the present cleaning composition, in neat form or diluted in a wash liquor, and then the situs is optionally washed and/or rinsed. For purposes of the present invention, “washing” includes but is not limited to, scrubbing, and mechanical agitation. In some embodiments, the cleaning compositions are typically employed at concentrations of from about 500 ppm to about 15,000 ppm in solution. When the wash solvent is water, the water temperature typically ranges from about 5° C. to about 90° C. and, when the situs comprises a fabric, the water to fabric mass ratio is typically from about 1:1 to about 30:1.

In additional embodiments, the present invention also provides compositions and methods utilizing various surfactants and surfactant blends to assess and improve the performance of proteases in detergent compositions. Using experimental design software, a simplex lattice mixture experiment was designed to evaluate the activity of a protease in the presence of the most commonly used surfactants in liquid laundry detergents; namely linear alkylbenzene sulfonate (LAS), alkylethoxy sulfate (AES), and alcohol ethoxylate (AE). LAS and AES are anionic surfactants, while AE is a nonionic surfactant.

Surprisingly, it was determined that selecting a surfactant composition for optimum performance of a protease was not simply a matter of selecting the surfactant in which the protease was most stable. Rather, selecting an optimum surfactant composition was based on combining different surfactants in a ratio that provided the best overall cleaning results, wherein the mixture included surfactants that if used in the absence of other surfactants, would destabilize the protease.

For example, it was determined that in some embodiments, a protease is able to function better in the presence of a first surfactant when a second surfactant is present but less well if a third surfactant is present. In additional embodiments, a protease tolerates much higher levels of a first surfactant, depending on the ratio of a second and third surfactant. The observation that enzymes can be used in the presence of different surfactants if the ratios of the surfactants are carefully selected is contrary to the conventional belief that enzymes must be used only in combination with surfactants that do not adversely affect their activity, limiting the use of enzymes to certain detergent compositions.

Based, in part, on the observations described herein, the present compositions and methods provide detergent composition comprising at least one protease and a mixture of surfactants in a ratio preselected to promote the activity of the protease, wherein the surfactants are not selected simply by measuring the stability of the protease in each surfactant. In some cases, the protease is inactivated or exhibits reduced activity in the presence of a different ratio of the same surfactants, or in the presence of any subset of the surfactants but in the absence of at least one of the surfactants in the mixture. In some cases, the protease is inactivated or exhibits reduced activity in the presence of any one of the surfactants, in the absence of other surfactant present in the mixture. Similarly, in some cases, the presence of a first surfactant allows the use of an increased amount of a second surfactant, wherein the same amount of the second surfactant in the absence of the first surfactant would inactivate or reduce the activity of the protease.

In addition, the presence of a first type of surfactant (e.g., a non-ionic or anionic detergent) permits the use of a second type of detergent, where the second type of detergent in the absence of the first type of surfactant would inactivate or reduce the activity of the protease.

In these experiments, Bacillus amyloliquefaciens subtilisin BPN′-Y217L (“FNA”; Genencor) was used, as well as variants of this enzyme. At low temperatures (i.e., 16° C.) the protease was active in a composition comprising a relatively small amount of AE and a larger amount of either AES or LAS, or both. In comparison, the protease was less active in a composition comprising only AES, only LAS, and particularly, only AE. Therefore, the preferred composition was not one that included only the single surfactant in which the protease was most active, but rather one that included at least two, and preferably all three surfactants, any one of which would inactivate or reduce the activity of the protease if used individually at a sufficient level. The particular ratio of AES>LAS>AE appeared to produce the best result for this protease at the low temperature.

In contrast, at high temperatures (i.e., 32° C.) the protease was active in a composition comprising only AES, or AES in combination with LAS and a relatively small amount of AE. Thus, the tolerance for AES increased at the higher temperature, making the inclusion of the other surfactants less important.

Several additional tests were also conducted. The protease activity after incubation was determined using AAPF-pNA substrate. The melting point, Tm, was measured of the enzyme in each detergent formulation. Finally, four formulations were selected and tested in the Terg-O-Tometer for correlation to the 96-well assay results (See, Example 22).

DEFINITIONS

Unless otherwise indicated, the practice of the present invention involves conventional techniques commonly used in molecular biology, protein engineering, microbiology, and recombinant DNA, which are within the skill of the art. Such techniques are known to those of skill in the art and are described in numerous texts and reference works (See e.g., Sambrook et al., “Molecular Cloning: A Laboratory Manual”, Second Edition (Cold Spring Harbor), [1989]); and Ausubel et al., “Current Protocols in Molecular Biology” [1987]). All patents, patent applications, articles and publications mentioned herein, both supra and infra, are hereby expressly incorporated herein by reference.

Unless defined otherwise herein, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. There are various dictionaries available and known to those in the art that provide definitions of these terms. Although any methods and materials similar or equivalent to those described herein find use in the practice of the present invention, the preferred methods and materials are described herein. Accordingly, the terms defined immediately below are more fully described by reference to the Specification as a whole. Also, as used herein, the singular “a”, “an” and “the” includes the plural reference unless the context clearly indicates otherwise. Numeric ranges are inclusive of the numbers defining the range. Unless otherwise indicated, nucleic acids are written left to right in 5′ to 3′ orientation; amino acid sequences are written left to right in amino to carboxy orientation, respectively. It is to be understood that this invention is not limited to the particular methodology, protocols, and reagents described, as these may vary, depending upon the context they are used by those of skill in the art.

The practice of the present invention employs, unless otherwise indicated, conventional techniques of protein purification, molecular biology, microbiology, recombinant DNA techniques and protein sequencing, all of which are within the skill of those in the art.

Furthermore, the headings provided herein are not limitations of the various aspects or embodiments of the invention which can be had by reference to the specification as a whole. Accordingly, the terms defined immediately below are more fully defined by reference to the specification as a whole. Nonetheless, in order to facilitate understanding of the invention, a number of terms are defined below.

As used herein, the terms “protease,” and “proteolytic activity” refer to a protein or peptide exhibiting the ability to hydrolyze peptides or substrates having peptide linkages. Many well known procedures exist for measuring proteolytic activity (Kalisz, “Microbial Proteinases,” In: Fiechter (ed.), Advances in Biochemical Engineering/Biotechnology, [1988]). For example, proteolytic activity may be ascertained by comparative assays which analyze the respective protease's ability to hydrolyze a commercial substrate. Exemplary substrates useful in the analysis of protease or proteolytic activity, include, but are not limited to di-methyl casein (Sigma C-9801), bovine collagen (Sigma C-9879), bovine elastin (Sigma E-1625), and bovine keratin (ICN Biomedical 902111). Colorimetric assays utilizing these substrates are well known in the art (See e.g., WO 99/34011; and U.S. Pat. No. 6,376,450, both of which are incorporated herein by reference). The pNA assay (See e.g., Del Mar et al., Anal. Biochem., 99:316-320 [1979]) also finds use in determining the active enzyme concentration for fractions collected during gradient elution. This assay measures the rate at which p-nitroaniline is released as the enzyme hydrolyzes the soluble synthetic substrate, succinyl-alanine-alanine-proline-phenylalanine-p-nitroanilide (sAAPF-pNA). The rate of production of yellow color from the hydrolysis reaction is measured at 410 nm on a spectrophotometer and is proportional to the active enzyme concentration. In addition, absorbance measurements at 280 nm can be used to determine the total protein concentration. The active enzyme/total-protein ratio gives the enzyme purity.

As used herein, “the genus Bacillus” includes all species within the genus “Bacillus,” as known to those of skill in the art, including but not limited to B. subtilis, B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. clausii, B. halodurans, B. megaterium, B. coagulans, B. circulans, B. lautus, and B. thuringiensis. It is recognized that the genus Bacillus continues to undergo taxonomical reorganization. Thus, it is intended that the genus include species that have been reclassified, including but not limited to such organisms as B. stearothermophilus, which is now named “Geobacillus stearothermophilus.” The production of resistant endospores in the presence of oxygen is considered the defining feature of the genus Bacillus, although this characteristic also applies to the recently named Alicyclobacillus, Amphibacillus, Aneurinibacillus, Anoxybacillus, Brevibacillus, Filobacillus, Gracilibacillus, Halobacillus, Paenibacillus, Salibacillus, Thermobacillus, Ureibacillus, and Virgibacillus.

The terms “polynucleotide” and “nucleic acid”, used interchangeably herein, refer to a polymeric form of nucleotides of any length, either ribonucleotides or deoxyribonucleotides. These terms include, but are not limited to, a single-, double- or triple-stranded DNA, genomic DNA, cDNA, RNA, DNA-RNA hybrid, or a polymer comprising purine and pyrimidine bases, or other natural, chemically, biochemically modified, non-natural or derivatized nucleotide bases. The following are non-limiting examples of polynucleotides: genes, gene fragments, chromosomal fragments, ESTs, exons, introns, mRNA, tRNA, rRNA, ribozymes, cDNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers. In some embodiments, polynucleotides comprise modified nucleotides, such as methylated nucleotides and nucleotide analogs, uracyl, other sugars and linking groups such as fluororibose and thioate, and nucleotide branches. In alternative embodiments, the sequence of nucleotides is interrupted by non-nucleotide components.

As used herein, the terms “DNA construct” and “transforming DNA” are used interchangeably to refer to DNA used to introduce sequences into a host cell or organism. The DNA may be generated in vitro by PCR or any other suitable technique(s) known to those in the art. In particularly preferred embodiments, the DNA construct comprises a sequence of interest (e.g., as an incoming sequence). In some embodiments, the sequence is operably linked to additional elements such as control elements (e.g., promoters, etc.). The DNA construct may further comprise a selectable marker. It may further comprise an incoming sequence flanked by homology boxes. In a further embodiment, the transforming DNA comprises other non-homologous sequences, added to the ends (e.g., stuffer sequences or flanks). In some embodiments, the ends of the incoming sequence are closed such that the transforming DNA forms a closed circle. The transforming sequences may be wild-type, mutant or modified. In some embodiments, the DNA construct comprises sequences homologous to the host cell chromosome. In other embodiments, the DNA construct comprises non-homologous sequences. Once the DNA construct is assembled in vitro it may be used to: 1) insert heterologous sequences into a desired target sequence of a host cell, and/or 2) mutagenize a region of the host cell chromosome (i.e., replace an endogenous sequence with a heterologous sequence), 3) delete target genes, and/or 4) introduce a replicating plasmid into the host.

As used herein, the terms “expression cassette” and “expression vector” refer to nucleic acid constructs generated recombinantly or synthetically, with a series of specified nucleic acid elements that permit transcription of a particular nucleic acid in a target cell. The recombinant expression cassette can be incorporated into a plasmid, chromosome, mitochondrial DNA, plastid DNA, virus, or nucleic acid fragment. Typically, the recombinant expression cassette portion of an expression vector includes, among other sequences, a nucleic acid sequence to be transcribed and a promoter. In preferred embodiments, expression vectors have the ability to incorporate and express heterologous DNA fragments in a host cell. Many prokaryotic and eukaryotic expression vectors are commercially available. Selection of appropriate expression vectors is within the knowledge of those of skill in the art. The term “expression cassette” is used interchangeably herein with “DNA construct,” and their grammatical equivalents. Selection of appropriate expression vectors is within the knowledge of those of skill in the art.

As used herein, the term “vector” refers to a polynucleotide construct designed to introduce nucleic acids into one or more cell types. Vectors include cloning vectors, expression vectors, shuttle vectors, plasmids, cassettes and the like. In some embodiments, the polynucleotide construct comprises a DNA sequence encoding the protease (e.g., precursor or mature protease) that is operably linked to a suitable prosequence (e.g., secretory, etc.) capable of effecting the expression of the DNA in a suitable host.

As used herein, the term “plasmid” refers to a circular double-stranded (ds) DNA construct used as a cloning vector, and which forms an extrachromosomal self-replicating genetic element in some eukaryotes or prokaryotes, or integrates into the host chromosome.

As used herein in the context of introducing a nucleic acid sequence into a cell, the term “introduced” refers to any method suitable for transferring the nucleic acid sequence into the cell. Such methods for introduction include but are not limited to protoplast fusion, transfection, transformation, conjugation, and transduction (See e.g., Ferrari et al., “Genetics,” in Hardwood et al, (eds.), Bacillus, Plenum Publishing Corp., pages 57-72, [1989]).

As used herein, the terms “transformed” and “stably transformed” refers to a cell that has a non-native (heterologous) polynucleotide sequence integrated into its genome or as an episomal plasmid that is maintained for at least two generations.

A nucleic acid is “operably linked” when it is placed into a functional relationship with another nucleic acid sequence. For example, DNA encoding a secretory leader (i.e., a signal peptide), is operably linked to DNA for a polypeptide if it is expressed as a preprotein that participates in the secretion of the polypeptide; a promoter or enhancer is operably linked to a coding sequence if it affects the transcription of the sequence; or a ribosome binding site is operably linked to a coding sequence if it is positioned so as to facilitate translation. Generally, “operably linked” means that the DNA sequences being linked are contiguous, and, in the case of a secretory leader, contiguous and in reading phase. However, enhancers do not have to be contiguous. Linking is accomplished by ligation at convenient restriction sites. If such sites do not exist, the synthetic oligonucleotide adaptors or linkers are used in accordance with conventional practice.

As used herein the term “gene” refers to a polynucleotide (e.g., a DNA segment), that encodes a polypeptide and includes regions preceding and following the coding regions as well as intervening sequences (introns) between individual coding segments (exons).

As used herein, “homologous genes” refers to a pair of genes from different, but usually related species, which correspond to each other and which are identical or very similar to each other. The term encompasses genes that are separated by speciation (i.e., the development of new species) (e.g., orthologous genes), as well as genes that have been separated by genetic duplication (e.g., paralogous genes).

As used herein, proteins are defined as having a common “fold” if they have the same major secondary structures in the same arrangement and with the same topological connections. Different proteins with the same fold often have peripheral elements of secondary structure and turn regions that differ in size and conformation. In some cases, these differing peripheral regions may comprise half the structure. Proteins placed together in the same fold category do not necessarily have a common evolutionary origin (e.g., structural similarities arising from the physics and chemistry of proteins favoring certain packing arrangements and chain topologies).

As used herein, “homology” refers to sequence similarity or identity, with identity being preferred. This homology is determined using standard techniques known in the art (See e.g., Smith and Waterman, Adv. Appl. Math., 2:482 [1981]; Needleman and Wunsch, J. Mol. Biol., 48:443 [1970]; Pearson and Lipman, Proc. Natl. Acad. Sci. USA 85:2444 [1988]; programs such as GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package (Genetics Computer Group, Madison, Wis.); and Devereux et al., Nucl. Acid Res., 12:387-395 [1984]).

As used herein, an “analogous sequence” is one wherein the function of the gene is essentially the same as the gene based on the BPN′ protease. Analogous sequences are determined by known methods of sequence alignment. A commonly used alignment method is BLAST, although as indicated above and below, there are other methods that also find use in aligning sequences.

One example of a useful algorithm is PILEUP. PILEUP creates a multiple sequence alignment from a group of related sequences using progressive, pair-wise alignments. It can also plot a tree showing the clustering relationships used to create the alignment. PILEUP uses a simplification of the progressive alignment method of Feng and Doolittle (Feng and Doolittle, J. Mol. Evol., 35:351-360 [1987]). The method is similar to that described by Higgins and Sharp (Higgins and Sharp, CABIOS 5:151-153 [1989]). Useful PILEUP parameters including a default gap weight of 3.00, a default gap length weight of 0.10, and weighted end gaps.

Another example of a useful algorithm is the BLAST algorithm, described by Altschul et al., (Altschul et al., J. Mol. Biol., 215:403-410, [1990]; and Karlin et al., Proc. Natl. Acad. Sci. USA 90:5873-5787 [1993]). A particularly useful BLAST program is the WU-BLAST-2 program (See, Altschul et al., Meth. Enzymol., 266:460-480 [1996]). WU-BLAST-2 uses several search parameters, most of which are set to the default values. The adjustable parameters are set with the following values: overlap span=1, overlap fraction=0.125, word threshold (T)=11. The HSP S and HSP S2 parameters are dynamic values and are established by the program itself depending upon the composition of the particular sequence and composition of the particular database against which the sequence of interest is being searched. However, the values may be adjusted to increase sensitivity. A % amino acid sequence identity value is determined by the number of matching identical residues divided by the total number of residues of the “longer” sequence in the aligned region. The “longer” sequence is the one having the most actual residues in the aligned region (gaps introduced by WU-Blast-2 to maximize the alignment score are ignored).

Thus, “percent (%) nucleic acid sequence identity” is defined as the percentage of nucleotide residues in a candidate sequence that are identical with the nucleotide residues of the starting sequence (i.e., the sequence of interest). A preferred method utilizes the BLASTN module of WU-BLAST-2 set to the default parameters, with overlap span and overlap fraction set to 1 and 0.125, respectively.

As used herein, “recombinant” includes reference to a cell or vector, that has been modified by the introduction of a heterologous nucleic acid sequence or that the cell is derived from a cell so modified. Thus, for example, recombinant cells express genes that are not found in identical form within the native (non-recombinant) form of the cell or express native genes that are otherwise abnormally expressed, under expressed or not expressed at all as a result of deliberate human intervention. “Recombination,” “recombining,” and generating a “recombined” nucleic acid are generally the assembly of two or more nucleic acid fragments wherein the assembly gives rise to a chimeric gene.

In some preferred embodiments, mutant DNA sequences are generated with site saturation mutagenesis in at least one codon. In another preferred embodiment, site saturation mutagenesis is performed for two or more codons. In a further embodiment, mutant DNA sequences have more than about 50%, more than about 55%, more than about 60%, more than about 65%, more than about 70%, more than about 75%, more than about 80%, more than about 85%, more than about 90%, more than about 95%, or more than about 98% homology with the wild-type sequence. In alternative embodiments, mutant DNA is generated in vivo using any known mutagenic procedure such as, for example, radiation, nitrosoguanidine and the like. The desired DNA sequence is then isolated and used in the methods provided herein.

As used herein, the terms “amplification” and “gene amplification” refer to a process by which specific DNA sequences are disproportionately replicated such that the amplified gene becomes present in a higher copy number than was initially present in the genome. In some embodiments, selection of cells by growth in the presence of a drug (e.g., an inhibitor of an inhibitable enzyme) results in the amplification of either the endogenous gene encoding the gene product required for growth in the presence of the drug or by amplification of exogenous (i.e., input) sequences encoding this gene product, or both.

“Amplification” is a special case of nucleic acid replication involving template specificity. It is to be contrasted with non-specific template replication (i.e., replication that is template-dependent but not dependent on a specific template). Template specificity is here distinguished from fidelity of replication (i.e., synthesis of the proper polynucleotide sequence) and nucleotide (ribo- or deoxyribo-) specificity. Template specificity is frequently described in terms of “target” specificity. Target sequences are “targets” in the sense that they are sought to be sorted out from other nucleic acid. Amplification techniques have been designed primarily for this sorting out.

As used herein, the term “primer” refers to an oligonucleotide, whether occurring naturally as in a purified restriction digest or produced synthetically, which is capable of acting as a point of initiation of synthesis when placed under conditions in which synthesis of a primer extension product which is complementary to a nucleic acid strand is induced, (i.e., in the presence of nucleotides and an inducing agent such as DNA polymerase and at a suitable temperature and pH). The primer is preferably single stranded for maximum efficiency in amplification, but may alternatively be double stranded. If double stranded, the primer is first treated to separate its strands before being used to prepare extension products. Preferably, the primer is an oligodeoxyribonucleotide. The primer must be sufficiently long to prime the synthesis of extension products in the presence of the inducing agent. The exact lengths of the primers will depend on many factors, including temperature, source of primer and the use of the method.

As used herein, the term “probe” refers to an oligonucleotide (i.e., a sequence of nucleotides), whether occurring naturally as in a purified restriction digest or produced synthetically, recombinantly or by PCR amplification, which is capable of hybridizing to another oligonucleotide of interest. A probe may be single-stranded or double-stranded. Probes are useful in the detection, identification and isolation of particular gene sequences. It is contemplated that any probe used in the present invention will be labeled with any “reporter molecule,” so that is detectable in any detection system, including, but not limited to enzyme (e.g., ELISA, as well as enzyme-based histochemical assays), fluorescent, radioactive, and luminescent systems. It is not intended that the present invention be limited to any particular detection system or label.

As used herein, the term “target,” when used in reference to the polymerase chain reaction, refers to the region of nucleic acid bounded by the primers used for polymerase chain reaction. Thus, the “target” is sought to be sorted out from other nucleic acid sequences. A “segment” is defined as a region of nucleic acid within the target sequence.

As used herein, the term “polymerase chain reaction” (“PCR”) refers to the methods of U.S. Pat. Nos. 4,683,195 4,683,202, and 4,965,188, hereby incorporated by reference, which include methods for increasing the concentration of a segment of a target sequence in a mixture of genomic DNA without cloning or purification. This process for amplifying the target sequence consists of introducing a large excess of two oligonucleotide primers to the DNA mixture containing the desired target sequence, followed by a precise sequence of thermal cycling in the presence of a DNA polymerase. The two primers are complementary to their respective strands of the double stranded target sequence. To effect amplification, the mixture is denatured and the primers then annealed to their complementary sequences within the target molecule. Following annealing, the primers are extended with a polymerase so as to form a new pair of complementary strands. The steps of denaturation, primer annealing and polymerase extension can be repeated many times (i.e., denaturation, annealing and extension constitute one “cycle”; there can be numerous “cycles”) to obtain a high concentration of an amplified segment of the desired target sequence. The length of the amplified segment of the desired target sequence is determined by the relative positions of the primers with respect to each other, and therefore, this length is a controllable parameter. By virtue of the repeating aspect of the process, the method is referred to as the “polymerase chain reaction” (hereinafter “PCR”). Because the desired amplified segments of the target sequence become the predominant sequences (in terms of concentration) in the mixture, they are said to be “PCR amplified”.

As used herein, the term “amplification reagents” refers to those reagents (deoxyribonucleotide triphosphates, buffer, etc.), needed for amplification except for primers, nucleic acid template and the amplification enzyme. Typically, amplification reagents along with other reaction components are placed and contained in a reaction vessel (test tube, microwell, etc.).

As used herein, the term “RT-PCR” refers to the replication and amplification of RNA sequences. In this method, reverse transcription is coupled to PCR, most often using a one enzyme procedure in which a thermostable polymerase is employed, as described in U.S. Pat. No. 5,322,770, herein incorporated by reference. In RT-PCR, the RNA template is converted to cDNA due to the reverse transcriptase activity of the polymerase, and then amplified using the polymerizing activity of the polymerase (i.e., as in other PCR methods).

As used herein, the terms “restriction endonucleases” and “restriction enzymes” refer to bacterial enzymes, each of which cut double-stranded DNA at or near a specific nucleotide sequence.

A “restriction site” refers to a nucleotide sequence recognized and cleaved by a given restriction endonuclease and is frequently the site for insertion of DNA fragments. In certain embodiments of the invention restriction sites are engineered into the selective marker and into 5′ and 3′ ends of the DNA construct.

“Homologous recombination” means the exchange of DNA fragments between two DNA molecules or paired chromosomes at the site of identical or nearly identical nucleotide sequences. In a preferred embodiment, chromosomal integration is homologous recombination.

As used herein “amino acid” refers to peptide or protein sequences or portions thereof. The terms “protein,” “peptide,” and “polypeptide” are used interchangeably.

As used herein, “protein of interest” and “polypeptide of interest” refer to a protein/polypeptide that is desired and/or being assessed. In some embodiments, the protein of interest is expressed intracellularly, while in other embodiments, it is a secreted polypeptide. In particularly preferred embodiments, these enzymes include the serine proteases of the present invention. In some embodiments, the protein of interest is a secreted polypeptide which is fused to a signal peptide (i.e., an amino-terminal extension on a protein to be secreted). Nearly all secreted proteins use an amino-terminal protein extension which plays a crucial role in the targeting to and translocation of precursor proteins across the membrane. This extension is proteolytically removed by a signal peptidase during or immediately following membrane transfer.

A polynucleotide is said to “encode” an RNA or a polypeptide if, in its native state or when manipulated by methods known to those of skill in the art, it can be transcribed and/or translated to produce the RNA, the polypeptide or a fragment thereof. The anti-sense strand of such a nucleic acid is also said to encode the sequences. As is known in the art, a DNA can be transcribed by an RNA polymerase to produce RNA, but an RNA can be reverse transcribed by reverse transcriptase to produce a DNA. Thus a DNA can encode a RNA and vice versa.

“Host strain” or “host cell” refers to a suitable host for an expression vector comprising DNA according to the present invention.

An enzyme is “overexpressed” in a host cell if the enzyme is expressed in the cell at a higher level that the level at which it is expressed in a corresponding wild-type cell.

The terms “protein” and “polypeptide” are used interchangeability herein. The 3-letter code for amino acids as defined in conformity with the IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN) is used through out this disclosure. It is also understood that a polypeptide may be coded for by more than one nucleotide sequence due to the degeneracy of the genetic code.

A “prosequence” is an amino acid sequence between the signal sequence and mature protease that is necessary for the secretion of the protease. Cleavage of the pro sequence results in a mature active protease.

The term “signal sequence” or “signal peptide” refers to any sequence of nucleotides and/or amino acids which may participate in the secretion of the mature or precursor forms of the protein. This definition of signal sequence is a functional one, meant to include all those amino acid sequences encoded by the N-terminal portion of the protein gene, which participate in the effectuation of the secretion of protein. They are often, but not universally, bound to the N-terminal portion of a protein or to the N-terminal portion of a precursor protein. The signal sequence may be endogenous or exogenous. The signal sequence may be that normally associated with the protein (e.g., protease), or may be from a gene encoding another secreted protein. One exemplary exogenous signal sequence comprises the first seven amino acid residues of the signal sequence from Bacillus subtilis subtilisin fused to the remainder of the signal sequence of the subtilisin from Bacillus lentus (ATCC 21536).

The term “hybrid signal sequence” refers to signal sequences in which part of sequence is obtained from the expression host fused to the signal sequence of the gene to be expressed. In some embodiments, synthetic sequences are utilized.

The term “mature” form of a protein or peptide refers to the final functional form of the protein or peptide. For example, a mature form of the protease of the present invention includes at least the amino acid sequence identical to residue positions 1-275 of SEQ ID NO:2.

The term “precursor” form of a protein or peptide refers to a mature form of the protein having a prosequence operably linked to the amino or carbonyl terminus of the protein. The precursor may also have a “signal” sequence operably linked, to the amino terminus of the prosequence. The precursor may also have additional polynucleotides that are involved in post-translational activity (e.g., polynucleotides cleaved therefrom to leave the mature form of a protein or peptide).

“Naturally occurring enzyme” refers to an enzyme having the unmodified amino acid sequence identical to that found in nature. Naturally occurring enzymes include native enzymes, those enzymes naturally expressed or found in the particular microorganism.

The terms “derived from” and “obtained from” refer to not only a protease produced or producible by a strain of the organism in question, but also a protease encoded by a DNA sequence isolated from such strain and produced in a host organism containing such DNA sequence. Additionally, the term refers to a protease which is encoded by a DNA sequence of synthetic and/or cDNA origin and which has the identifying characteristics of the protease in question.

A “derivative” within the scope of this definition generally retains the characteristic proteolytic activity observed in the wild-type, native or parent form to the extent that the derivative is useful for similar purposes as the wild-type, native or parent form. Functional derivatives of serine protease encompass naturally occurring, synthetically or recombinantly produced peptides or peptide fragments which have the general characteristics of the serine protease of the present invention.

The term “functional derivative” refers to a derivative of a nucleic acid which has the functional characteristics of a nucleic acid which encodes serine protease. Functional derivatives of a nucleic acid which encode serine protease of the present invention encompass naturally occurring, synthetically or recombinantly produced nucleic acids or fragments and encode serine protease characteristic of the present invention. Wild type nucleic acid encoding serine proteases according to the invention include naturally occurring alleles and homologues based on the degeneracy of the genetic code known in the art.

The term “identical” in the context of two nucleic acids or polypeptide sequences refers to the residues in the two sequences that are the same when aligned for maximum correspondence, as measured using one of the following sequence comparison or analysis algorithms.

The term “optimal alignment” refers to the alignment giving the highest percent identity score.

“Percent sequence identity,” “percent amino acid sequence identity,” “percent gene sequence identity,” and/or “percent nucleic acid/polynucleotide sequence identity,” with respect to two amino acid, polynucleotide and/or gene sequences (as appropriate), refer to the percentage of residues that are identical in the two sequences when the sequences are optimally aligned. Thus, 80% amino acid sequence identity means that 80% of the amino acids in two optimally aligned polypeptide sequences are identical.

The phrase “substantially identical” in the context of two nucleic acids or polypeptides thus refers to a polynucleotide or polypeptide that comprising at least about 70% sequence identity, preferably at least about 75%, preferably at least about 80%, preferably at least about 85%, preferably at least about 90%, preferably at least about 95%, preferably at least about 97%, preferably at least about 98%, and preferably at least about 99% sequence identity as compared to a reference sequence using the programs or algorithms (e.g., BLAST, ALIGN, CLUSTAL) using standard parameters. One indication that two polypeptides are substantially identical is that the first polypeptide is immunologically cross-reactive with the second polypeptide. Typically, polypeptides that differ by conservative amino acid substitutions are immunologically cross-reactive. Thus, a polypeptide is substantially identical to a second polypeptide, for example, where the two peptides differ only by a conservative substitution. Another indication that two nucleic acid sequences are substantially identical is that the two molecules hybridize to each other under stringent conditions (e.g., within a range of medium to high stringency).

The phrase “equivalent,” in this context, refers to serine proteases enzymes that are encoded by a polynucleotide capable of hybridizing to the polynucleotide having the sequence as shown in SEQ ID NO:1, under conditions of medium to maximum stringency. For example, being equivalent means that an equivalent mature serine protease comprises at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 91%, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, and/or at least about 99% sequence identity to the mature BPN′ serine protease having the amino acid sequence of SEQ ID NO:2.

The term “isolated” or “purified” refers to a material that is removed from its original environment (e.g., the natural environment if it is naturally occurring). For example, the material is said to be “purified” when it is present in a particular composition in a higher or lower concentration than exists in a naturally occurring or wild type organism or in combination with components not normally present upon expression from a naturally occurring or wild type organism. For example, a naturally-occurring polynucleotide or polypeptide present in a living animal is not isolated, but the same polynucleotide or polypeptide, separated from some or all of the coexisting materials in the natural system, is isolated. In some embodiments, such polynucleotides are part of a vector, and/or such polynucleotides or polypeptides are part of a composition, and still be isolated in that such vector or composition is not part of its natural environment. In preferred embodiments, a nucleic acid or protein is said to be purified, for example, if it gives rise to essentially one band in an electrophoretic gel or blot.

The term “isolated”, when used in reference to a DNA sequence, refers to a DNA sequence that has been removed from its natural genetic milieu and is thus free of other extraneous or unwanted coding sequences, and is in a form suitable for use within genetically engineered protein production systems. Such isolated molecules are those that are separated from their natural environment and include cDNA and genomic clones. Isolated DNA molecules of the present invention are free of other genes with which they are ordinarily associated, but may include naturally occurring 5′ and 3′ untranslated regions such as promoters and terminators. The identification of associated regions will be evident to one of ordinary skill in the art (See e.g., Dynan and Tijan, Nature 316:774-78 [1985]). The term “an isolated DNA sequence” is alternatively referred to as “a cloned DNA sequence”.

The term “isolated,” when used in reference to a protein, refers to a protein that is found in a condition other than its native environment. In a preferred form, the isolated protein is substantially free of other proteins, particularly other homologous proteins. An isolated protein is more than about 10% pure, preferably more than about 20% pure, and even more preferably more than about 30% pure, as determined by SDS-PAGE. Further aspects of the invention encompass the protein in a highly purified form (i.e., more than about 40% pure, more than about 60% pure, more than about 80% pure, more than about 90% pure, more than about 95% pure, more than about 97% pure, and even more than about 99% pure), as determined by SDS-PAGE.

As used herein, the term, “combinatorial mutagenesis” refers to methods in which libraries of variants of a starting sequence are generated. In these libraries, the variants contain one or several mutations chosen from a predefined set of mutations. In addition, the methods provide means to introduce random mutations which were not members of the predefined set of mutations. In some embodiments, the methods include those set forth in U.S. patent application Ser. No. 09/699,250, filed Oct. 26, 2000, hereby incorporated by reference. In alternative embodiments, combinatorial mutagenesis methods encompass commercially available kits (e.g., QuikChange® Multisite, Stratagene, San Diego, Calif.).

As used herein, the term “library of mutants” refers to a population of cells which are identical in most of their genome but include different homologues of one or more genes. Such libraries can be used, for example, to identify genes or operons with improved traits.

As used herein, the term “starting gene” refers to a gene of interest that encodes a protein of interest that is to be improved and/or changed using the present invention.

As used herein, the term “multiple sequence alignment” (“MSA”) refers to the sequences of multiple homologs of a starting gene that are aligned using an algorithm (e.g., Clustal W).

As used herein, the terms “consensus sequence” and “canonical sequence” refer to an archetypical amino acid sequence against which all variants of a particular protein or sequence of interest are compared. The terms also refer to a sequence that sets forth the nucleotides that are most often present in a DNA sequence of interest. For each position of a gene, the consensus sequence gives the amino acid that is most abundant in that position in the MSA.

As used herein, the term “consensus mutation” refers to a difference in the sequence of a starting gene and a consensus sequence. Consensus mutations are identified by comparing the sequences of the starting gene and the consensus sequence resulting from an MSA. In some embodiments, consensus mutations are introduced into the starting gene such that it becomes more similar to the consensus sequence. Consensus mutations also include amino acid changes that change an amino acid in a starting gene to an amino acid that is more frequently found in an MSA at that position relative to the frequency of that amino acid in the starting gene. Thus, the term consensus mutation comprises all single amino acid changes that replace an amino acid of the starting gene with an amino acid that is more abundant than the amino acid in the MSA.

As used herein, the term “initial hit” refers to a variant that was identified by screening a combinatorial consensus mutagenesis library. In preferred embodiments, initial hits have improved performance characteristics, as compared to the starting gene.

As used herein, the term “improved hit” refers to a variant that was identified by screening an enhanced combinatorial consensus mutagenesis library.

As used herein, the terms “improving mutation” and “performance-enhancing mutation” refer to a mutation that leads to improved performance when it is introduced into the starting gene. In some preferred embodiments, these mutations are identified by sequencing hits that were identified during the screening step of the method. In most embodiments, mutations that are more frequently found in hits are likely to be improving mutations, as compared to an unscreened combinatorial consensus mutagenesis library.

As used herein, the term “enhanced combinatorial consensus mutagenesis library” refers to a CCM library that is designed and constructed based on screening and/or sequencing results from an earlier round of CCM mutagenesis and screening. In some embodiments, the enhanced CCM library is based on the sequence of an initial hit resulting from an earlier round of CCM. In additional embodiments, the enhanced CCM is designed such that mutations that were frequently observed in initial hits from earlier rounds of mutagenesis and screening are favored. In some preferred embodiments, this is accomplished by omitting primers that encode performance-reducing mutations or by increasing the concentration of primers that encode performance-enhancing mutations relative to other primers that were used in earlier CCM libraries.

As used herein, the term “performance-reducing mutations” refer to mutations in the combinatorial consensus mutagenesis library that are less frequently found in hits resulting from screening as compared to an unscreened combinatorial consensus mutagenesis library. In preferred embodiments, the screening process removes and/or reduces the abundance of variants that contain “performance-reducing mutations.”

As used herein, the term “functional assay” refers to an assay that provides an indication of a protein's activity. In particularly preferred embodiments, the term refers to assay systems in which a protein is analyzed for its ability to function in its usual capacity. For example, in the case of enzymes, a functional assay involves determining the effectiveness of the enzyme in catalyzing a reaction. As used herein, the term “target property” refers to the property of the starting gene that is to be altered. It is not intended that the present invention be limited to any particular target property. However, in some preferred embodiments, the target property is the stability of a gene product (e.g., resistance to denaturation, proteolysis or other degradative factors), while in other embodiments, the level of production in a production host is altered. Indeed, it is contemplated that any property of a starting gene will find use in the present invention.

The term “property” or grammatical equivalents thereof in the context of a nucleic acid, as used herein, refer to any characteristic or attribute of a nucleic acid that can be selected or detected. These properties include, but are not limited to, a property affecting binding to a polypeptide, a property conferred on a cell comprising a particular nucleic acid, a property affecting gene transcription (e.g., promoter strength, promoter recognition, promoter regulation, enhancer function), a property affecting RNA processing (e.g., RNA splicing, RNA stability, RNA conformation, and post-transcriptional modification), a property affecting translation (e.g., level, regulation, binding of mRNA to ribosomal proteins, post-translational modification). For example, a binding site for a transcription factor, polymerase, regulatory factor, etc., of a nucleic acid may be altered to produce desired characteristics or to identify undesirable characteristics.

The term “property” or grammatical equivalents thereof in the context of a polypeptide (including proteins), as used herein, refer to any characteristic or attribute of a polypeptide that can be selected or detected. These properties include, but are not limited to oxidative stability, substrate specificity, catalytic activity, thermal stability, alkaline stability, pH activity profile, resistance to proteolytic degradation, K_(M), k_(cat), k_(cat)/k_(M) ratio, protein folding, inducing an immune response, ability to bind to a ligand, ability to bind to a receptor, ability to be secreted, ability to be displayed on the surface of a cell, ability to oligomerize, ability to signal, ability to stimulate cell proliferation, ability to inhibit cell proliferation, ability to induce apoptosis, ability to be modified by phosphorylation or glycosylation, and/or ability to treat disease, etc.

As used herein, the term “screening” has its usual meaning in the art and is, in general a multi-step process. In the first step, a mutant nucleic acid or variant polypeptide therefrom is provided. In the second step, a property of the mutant nucleic acid or variant polypeptide is determined. In the third step, the determined property is compared to a property of the corresponding precursor nucleic acid, to the property of the corresponding naturally occurring polypeptide or to the property of the starting material (e.g., the initial sequence) for the generation of the mutant nucleic acid.

It will be apparent to the skilled artisan that the screening procedure for obtaining a nucleic acid or protein with an altered property depends upon the property of the starting material the modification of which the generation of the mutant nucleic acid is intended to facilitate. The skilled artisan will therefore appreciate that the invention is not limited to any specific property to be screened for and that the following description of properties lists illustrative examples only. Methods for screening for any particular property are generally described in the art. For example, one can measure binding, pH, specificity, etc., before and after mutation, wherein a change indicates an alteration. Preferably, the screens are performed in a high-throughput manner, including multiple samples being screened simultaneously, including, but not limited to assays utilizing chips, phage display, and multiple substrates and/or indicators.

As used herein, in some embodiments, screens encompass selection steps in which variants of interest are enriched from a population of variants. Examples of these embodiments include the selection of variants that confer a growth advantage to the host organism, as well as phage display or any other method of display, where variants can be captured from a population of variants based on their binding or catalytic properties. In a preferred embodiment, a library of variants is exposed to stress (heat, protease, denaturation) and subsequently variants that are still intact are identified in a screen or enriched by selection. It is intended that the term encompass any suitable means for selection. Indeed, it is not intended that the present invention be limited to any particular method of screening.

As used herein, the term “targeted randomization” refers to a process that produces a plurality of sequences where one or several positions have been randomized. In some embodiments, randomization is complete (i.e., all four nucleotides, A, T, G, and C can occur at a randomized position. In alternative embodiments, randomization of a nucleotide is limited to a subset of the four nucleotides. Targeted randomization can be applied to one or several codons of a sequence, coding for one or several proteins of interest. When expressed, the resulting libraries produce protein populations in which one or more amino acid positions can contain a mixture of all 20 amino acids or a subset of amino acids, as determined by the randomization scheme of the randomized codon. In some embodiments, the individual members of a population resulting from targeted randomization differ in the number of amino acids, due to targeted or random insertion or deletion of codons. In further embodiments, synthetic amino acids are included in the protein populations produced. In some preferred embodiments, the majority of members of a population resulting from targeted randomization show greater sequence homology to the consensus sequence than the starting gene. In some embodiments, the sequence encodes one or more proteins of interest. In alternative embodiments, the proteins have differing biological functions. In some preferred embodiments, the incoming sequence comprises at least one selectable marker. This sequence can code for one or more proteins of interest. It can have other biological function. In many cases the incoming sequence will include a selectable marker, such as a gene that confers resistance to an antibiotic.

The terms “modified sequence” and “modified genes” are used interchangeably herein to refer to a sequence that includes a deletion, insertion or interruption of naturally occurring nucleic acid sequence. In some preferred embodiments, the expression product of the modified sequence is a truncated protein (e.g., if the modification is a deletion or interruption of the sequence). In some particularly preferred embodiments, the truncated protein retains biological activity. In alternative embodiments, the expression product of the modified sequence is an elongated protein (e.g., modifications comprising an insertion into the nucleic acid sequence). In some embodiments, an insertion leads to a truncated protein (e.g., when the insertion results in the formation of a stop codon). Thus, an insertion may result in either a truncated protein or an elongated protein as an expression product.

As used herein, the terms “mutant sequence” and “mutant gene” are used interchangeably and refer to a sequence that has an alteration in at least one codon occurring in a host cell's wild-type sequence. The expression product of the mutant sequence is a protein with an altered amino acid sequence relative to the wild-type. The expression product may have an altered functional capacity (e.g., enhanced enzymatic activity).

The terms “mutagenic primer” or “mutagenic oligonucleotide” (used interchangeably herein) are intended to refer to oligonucleotide compositions which correspond to a portion of the template sequence and which are capable of hybridizing thereto. With respect to mutagenic primers, the primer will not precisely match the template nucleic acid, the mismatch or mismatches in the primer being used to introduce the desired mutation into the nucleic acid library. As used herein, “non-mutagenic primer” or “non-mutagenic oligonucleotide” refers to oligonucleotide compositions which will match precisely to the template nucleic acid. In one embodiment of the invention, only mutagenic primers are used. In another preferred embodiment of the invention, the primers are designed so that for at least one region at which a mutagenic primer has been included, there is also non-mutagenic primer included in the oligonucleotide mixture. By adding a mixture of mutagenic primers and non-mutagenic primers corresponding to at least one of the mutagenic primers, it is possible to produce a resulting nucleic acid library in which a variety of combinatorial mutational patterns are presented. For example, if it is desired that some of the members of the mutant nucleic acid library retain their precursor sequence at certain positions while other members are mutant at such sites, the non-mutagenic primers provide the ability to obtain a specific level of non-mutant members within the nucleic acid library for a given residue. The methods of the invention employ mutagenic and non-mutagenic oligonucleotides which are generally between 10-50 bases in length, more preferably about 15-45 bases in length. However, it may be necessary to use primers that are either shorter than 10 bases or longer than 50 bases to obtain the mutagenesis result desired. With respect to corresponding mutagenic and non-mutagenic primers, it is not necessary that the corresponding oligonucleotides be of identical length, but only that there is overlap in the region corresponding to the mutation to be added. Primers may be added in a pre-defined ratio according to the present invention. For example, if it is desired that the resulting library have a significant level of a certain specific mutation and a lesser amount of a different mutation at the same or different site, by adjusting the amount of primer added, it is possible to produce the desired biased library. Alternatively, by adding lesser or greater amounts of non-mutagenic primers, it is possible to adjust the frequency with which the corresponding mutation(s) are produced in the mutant nucleic acid library.

As used herein, the phrase “contiguous mutations” refers to mutations which are presented within the same oligonucleotide primer. For example, contiguous mutations may be adjacent or nearby each other, however, they will be introduced into the resulting mutant template nucleic acids by the same primer.

As used herein, the phrase “discontiguous mutations” refers to mutations which are presented in separate oligonucleotide primers. For example, discontiguous mutations will be introduced into the resulting mutant template nucleic acids by separately prepared oligonucleotide primers.

The terms “wild-type sequence,” or “wild-type gene” are used interchangeably herein, to refer to a sequence that is native or naturally occurring in a host cell. In some embodiments, the wild-type sequence refers to a sequence of interest that is the starting point of a protein engineering project. The wild-type sequence may encode either a homologous or heterologous protein. A homologous protein is one the host cell would produce without intervention. A heterologous protein is one that the host cell would not produce but for the intervention.

Unless otherwise indicated, the amino acid position numbers refer to those assigned to the mature Bacillus amyloliquefaciens subtilisin sequence of SEQ ID NO:2. The invention, however, is not limited to the mutation of this particular subtilisin but extends to precursor proteases containing amino acid residues at positions which are “equivalent” to the particular identified residues in the Bacillus amyloliquefaciens subtilisin.

As used herein, the terms “modification” and “mutation” refers to any change or alteration in an amino acid sequence. It is intended that the term encompass substitutions, deletions, insertions, and/or replacement of amino acid side chains in an amino acid sequence of interest (e.g., a subtilisin sequence). It is also intended that the term encompass chemical modification of an amino acid sequence of interest (e.g., a subtilisin sequence).

As used herein, the term “antibodies” refers to immunoglobulins. Antibodies include but are not limited to immunoglobulins obtained directly from any species from which it is desirable to produce antibodies. In addition, the present invention encompasses modified antibodies. The term also refers to antibody fragments that retain the ability to bind to the epitope that the intact antibody binds and include polyclonal antibodies, monoclonal antibodies, chimeric antibodies, anti-idiotype (anti-ID) antibodies. Antibody fragments include, but are not limited to the complementarity-determining regions (CDRs), single-chain fragment variable regions (scFv), heavy chain variable region (VH), light chain variable region (VL). Polyclonal and monoclonal antibodies are also encompassed by the present invention. Preferably, the antibodies are monoclonal antibodies.

The term “oxidation stable” refers to proteases of the present invention that retain a specified amount of enzymatic activity over a given period of time under conditions prevailing during the proteolytic, hydrolyzing, cleaning or other process of the invention, for example while exposed to or contacted with bleaching agents or oxidizing agents. In some embodiments, the proteases retain at least about 50%, about 60%, about 70%, about 75%, about 80%, about 85%, about 90%, about 92%, about 95%, about 96%, about 97%, about 98%, or about 99% proteolytic activity after contact with a bleaching or oxidizing agent over a given time period, for example, at least about 1 minute, about 3 minutes, about 5 minutes, about 8 minutes, about 12 minutes, about 16 minutes, about 20 minutes, etc. In some embodiments, the stability is measured as described in the Examples.

The term “chelator stable” refers to proteases of the present invention that retain a specified amount of enzymatic activity over a given period of time under conditions prevailing during the proteolytic, hydrolyzing, cleaning or other process of the invention, for example while exposed to or contacted with chelating agents. In some embodiments, the proteases retain at least about 50%, about 60%, about 70%, about 75%, about 80%, about 85%, about 90%, about 92%, about 95%, about 96%, about 97%, about 98%, or about 99% proteolytic activity after contact with a chelating agent over a given time period, for example, at least about 10 minutes, about 20 minutes, about 40 minutes, about 60 minutes, about 100 minutes, etc. In some embodiments, the chelator stability is measured as described in the Examples.

The terms “thermally stable” and “thermostable” refer to proteases of the present invention that retain a specified amount of enzymatic activity after exposure to identified temperatures over a given period of time under conditions prevailing during the proteolytic, hydrolyzing, cleaning or other process of the invention, for example while exposed altered temperatures. Altered temperatures includes increased or decreased temperatures. In some embodiments, the proteases retain at least about 50%, about 60%, about 70%, about 75%, about 80%, about 85%, about 90%, about 92%, about 95%, about 96%, about 97%, about 98%, or about 99% proteolytic activity after exposure to altered temperatures over a given time period, for example, at least about 60 minutes, about 120 minutes, about 180 minutes, about 240 minutes, about 300 minutes, etc. In some embodiments, the thermostability is determined as described in the Examples.

The term “enhanced stability” in the context of an oxidation, chelator, thermal and/or pH stable protease refers to a higher retained proteolytic activity over time as compared to other serine proteases (e.g., subtilisin proteases) and/or wild-type enzymes.

The term “diminished stability” in the context of an oxidation, chelator, thermal and/or pH stable protease refers to a lower retained proteolytic activity over time as compared to other serine proteases (e.g., subtilisin proteases) and/or wild-type enzymes.

The term “cleaning activity” refers to the cleaning performance achieved by the protease under conditions prevailing during the proteolytic, hydrolyzing, cleaning or other process of the invention. In some embodiments, cleaning performance is determined by the application of various cleaning assays concerning enzyme sensitive stains, for example grass, blood, milk, or egg protein as determined by various chromatographic, spectrophotometric or other quantitative methodologies after subjection of the stains to standard wash conditions. Exemplary assays include, but are not limited to those described in WO 99/34011, and U.S. Pat. No. 6,605,458 (both of which are herein incorporated by reference), as well as those methods included in the Examples.

The term “cleaning effective amount” of a protease refers to the quantity of protease described hereinbefore that achieves a desired level of enzymatic activity in a specific cleaning composition. Such effective amounts are readily ascertained by one of ordinary skill in the art and are based on many factors, such as the particular protease used, the cleaning application, the specific composition of the cleaning composition, and whether a liquid or dry (e.g., granular, bar) composition is required, etc.

The term “cleaning adjunct materials,” as used herein, means any liquid, solid or gaseous material selected for the particular type of cleaning composition desired and the form of the product (e.g., liquid, granule, powder, bar, paste, spray, tablet, gel; or foam composition), which materials are also preferably compatible with the protease enzyme used in the composition. In some embodiments, granular compositions are in “compact” form, while in other embodiments, the liquid compositions are in a “concentrated” form.

The term “enhanced performance” in the context of cleaning activity refers to an increased or greater cleaning activity of certain enzyme sensitive stains such as egg, milk, grass or blood, as determined by usual evaluation after a standard wash cycle and/or multiple wash cycles.

The term “diminished performance” in the context of cleaning activity refers to an decreased or lesser cleaning activity of certain enzyme sensitive stains such as egg, milk, grass or blood, as determined by usual evaluation after a standard wash cycle.

The term “comparative performance” in the context of cleaning activity refers to at least about 60%, at least about 70%, at least about 80% at least about 90%, or at least about 95% of the cleaning activity of a comparative subtilisin protease (e.g., commercially available proteases), including but not limited to OPTIMASE™ protease (Genencor), PURAFECT™ protease products (Genencor), SAVINASE™ protease (Novozymes), BPN′-variants (See e.g., U.S. Pat. No. Re 34,606), RELASE™, DURAZYME™, EVERLASE™, KANNASE™ protease (Novozymes), MAXACAL™, MAXAPEMT™, PROPERASE™ proteases (Genencor; See also, U.S. Pat. No. Re 34,606, and U.S. Pat. Nos. 5,700,676; 5,955,340; 6,312,936; and 6,482,628), and B. lentus variant protease products (e.g., those described in WO 92/21760, WO 95/23221 and/or WO 97/07770). Exemplary subtilisin protease variants include, but are not limited to those having substitutions or deletions at residue positions equivalent to positions 76, 101, 103, 104, 120, 159, 167, 170, 194, 195, 217, 232, 235, 236, 245, 248, and/or 252 of BPN′. Cleaning performance can be determined by comparing the proteases of the present invention with those subtilisin proteases in various cleaning assays concerning enzyme sensitive stains such as grass, blood or milk as determined by usual spectrophotometric or analytical methodologies after standard wash cycle conditions.

As used herein, “fabric cleaning compositions” include hand and machine laundry detergent compositions including laundry additive compositions and compositions suitable for use in the soaking and/or pretreatment of stained fabrics (e.g., clothes, linens, and other textile materials).

As used herein, “non-fabric cleaning compositions” include non-textile (i.e., fabric) surface cleaning compositions, including but not limited to dishwashing detergent compositions, oral cleaning compositions, denture cleaning compositions, and personal cleansing compositions.

The “compact” form of the cleaning compositions herein is best reflected by density and, in terms of composition, by the amount of inorganic filler salt. Inorganic filler salts are conventional ingredients of detergent compositions in powder form. In conventional detergent compositions, the filler salts are present in substantial amounts, typically about 17 to about 35% by weight of the total composition. In contrast, in compact compositions, the filler salt is present in amounts not exceeding about 15% of the total composition. In some embodiments, the filler salt is present in amounts that do not exceed about 10%, or more preferably, about 5%, by weight of the composition. In some embodiments, the inorganic filler salts are selected from the alkali and alkaline-earth-metal salts of sulfates and chlorides. A preferred filler salt is sodium sulfate.

As used herein, the term “surfactant” refers to any compound generally recognized in the art as having surface active qualities. Surfactants generally include anionic, cationic, nonionic, and zwitterionic compounds, which are further described, herein.

As used herein, the terms “contacting” and “exposing” refer to placing a surfactant and lipolytic enzyme in sufficient proximity an oily stain or oily soil to enable the enzyme and surfactant to at least partially decrease the amount of the stain or soil by producing fatty acids that are solubilized in the surfactant. Contacting may occur in a washing machine, a sink, on a body surface, etc.

EXPERIMENTAL

The present invention is described in further detail in the following Examples which are not in any way intended to limit the scope of the invention as claimed. The attached Figures are meant to be considered as integral parts of the specification and description of the invention. The following Examples are offered to illustrate, but not to limit the claimed invention In the experimental disclosure which follows, the following abbreviations apply: ppm (parts per million); M (molar); mM (millimolar); μM (micromolar); nM (nanomolar); mol (moles); mmol (millimoles); μmol (micromoles); nmol (nanomoles); gm (grams); mg (milligrams); μg (micrograms); pg (picograms); L (liters); ml and mL (milliliters); μl and μL (microliters); cm (centimeters); mm (millimeters); μm (micrometers); nm (nanometers); U (units); V (volts); MW (molecular weight); sec (seconds); min(s) (minute/minutes); h(s) and hr(s) (hour/hours); ° C. (degrees Centigrade); QS (quantity sufficient); ND (not done); NA (not applicable); rpm (revolutions per minute); H₂O (water); dH₂O (deionized water); (HCl (hydrochloric acid); aa (amino acid); by (base pair); kb (kilobase pair); kD (kilodaltons); cDNA (copy or complementary DNA); DNA (deoxyribonucleic acid); ssDNA (single stranded DNA); dsDNA (double stranded DNA); dNTP (deoxyribonucleotide triphosphate); RNA (ribonucleic acid); MgCl₂ (magnesium chloride); NaCl (sodium chloride); w/v (weight to volume); v/v (volume to volume); g (gravity); OD (optical density); PI (performance index); Dulbecco's phosphate buffered solution (DPBS); SOC (2% Bacto-Tryptone, 0.5% Bacto Yeast Extract, 10 mM NaCl, 2.5 mM KCl); Terrific Broth (TB; 12 g/l Bacto Tryptone, 24 g/l glycerol, 2.31 g/l KH₂PO₄, and 12.54 g/l K₂HPO₄); OD₂₈₀ (optical density at 280 nm); OD₆₀₀ (optical density at 600 nm); A₄₀₅ (absorbance at 405 nm); Vmax (the maximum initial velocity of an enzyme catalyzed reaction); PAGE (polyacrylamide gel electrophoresis); PBS (phosphate buffered saline [150 mM NaCl, 10 mM sodium phosphate buffer, pH 7.2]); PBST (PBS+0.25% TWEEN® 20); PEG (polyethylene glycol); PCR (polymerase chain reaction); RT-PCR (reverse transcription PCR); SDS (sodium dodecyl sulfate); Tris (tris(hydroxymethyl)aminomethane); HEPES (N-[2-Hydroxyethyl]piperazine-N-[2-ethanesulfonic acid]); HBS (HEPES buffered saline); Tris-HCl (tris[Hydroxymethyl]aminomethane-hydrochloride); Tricine (N-[tris-(hydroxymethyl)-methyl]-glycine); CHES (2-(N-cyclo-hexylamino) ethane-sulfonic acid); TAPS (3-{[tris-(hydroxymethyl)-methyl]-amino}-propanesulfonic acid); CAPS (3-(cyclo-hexylamino)-propane-sulfonic acid; DMSO (dimethyl sulfoxide); DTT (1,4-dithio-DL-threitol); SA (sinapinic acid (s,5-dimethoxy-4-hydroxy cinnamic acid); TCA (trichloroacetic acid); Glut and GSH (reduced glutathione); GSSG (oxidized glutathione); TCEP (Tris[2-carboxyethyl] phosphine); Ci (Curies); mCi (milliCuries); μCi (microcuries); HPLC (high pressure liquid chromatography); RP-HPLC (reverse phase high pressure liquid chromatography); TLC (thin layer chromatography); MALDI-TOF (matrix-assisted laser desorption/ionization—time of flight); Ts (tosyl); Bn (benzyl); Ph (phenyl); Ms (mesyl); Et (ethyl), Me (methyl); Taq (Thermus aquaticus DNA polymerase); Klenow (DNA polymerase I large (Klenow) fragment); EGTA (ethylene glycol-bis(β-aminoethyl ether) N,N,N′,N′-tetraacetic acid); EDTA (ethylenediaminetetracetic acid); bla (β-lactamase or ampicillin-resistance gene); HDL (high density liquid); MJ Research (MJ Research, Reno, Nev.); Baseclear (Baseclear BV, Inc., Leiden, the Netherlands); PerSeptive (PerSeptive Biosystems, Framingham, Mass.); ThermoFinnigan (ThermoFinnigan, San Jose, Calif.); Argo (Argo BioAnalytica, Morris Plains, N.J.); Seitz EKS (SeitzSchenk Filtersystems GmbH, Bad Kreuznach, Germany); Pall (Pall Corp., East Hills, N.Y.); Spectrum (Spectrum Laboratories, Dominguez Rancho, Calif.); Molecular Structure (Molecular Structure Corp., Woodlands, Tex.); Accelrys (Accelrys, Inc., San Diego, Calif.); Chemical Computing (Chemical Computing Corp., Montreal, Canada); New Brunswick (New Brunswick Scientific, Co., Edison, N.J.); CFT (Center for Test Materials, Vlaardingen, the Netherlands); Test Fabrics (Test Fabrics, Inc., West Pittiston, Pa.), Procter & Gamble (Procter & Gamble, Inc., Cincinnati, Ohio); GE Healthcare (GE Healthcare, Chalfont St. Giles, United Kingdom); OXOID (Oxoid, Basingstoke, Hampshire, UK); Megazyme (Megazyme International Ireland Ltd., Bray Business Park, Bray, Co., Wicklow, Ireland); Finnzymes (Finnzymes Oy, Espoo, Finland); Kelco (CP Kelco, Wilmington, Del.); Corning (Corning Life Sciences, Corning, N.Y.); (NEN (NEN Life Science Products, Boston, Mass.); Pharma AS (Pharma AS, Oslo, Norway); Dynal (Dynal, Oslo, Norway); Bio-Synthesis (Bio-Synthesis, Lewisville, Tex.); ATCC (American Type Culture Collection, Rockville, Md.); Gibco/BRL (Gibco/BRL, Grand Island, N.Y.); Sigma (Sigma Chemical Co., St. Louis, Mo.); Pharmacia (Pharmacia Biotech, Piscataway, N.J.); NCBI (National Center for Biotechnology Information); Applied Biosystems (Applied Biosystems, Foster City, Calif.); BD Biosciences and/or Clontech (BD Biosciences CLONTECH Laboratories, Palo Alto, Calif.); Operon Technologies (Operon Technologies, Inc., Alameda, Calif.); MWG Biotech (MWG Biotech, High Point, N.C.); Oligos Etc (Oligos Etc. Inc, Wilsonville, Oreg.); Bachem (Bachem Bioscience, Inc., King of Prussia, Pa.); Difco (Difco Laboratories, Detroit, Mich.); Mediatech (Mediatech, Herndon, Va.; Santa Cruz (Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.); Oxoid (Oxoid Inc., Ogdensburg, N.Y.); Worthington (Worthington Biochemical Corp., Freehold, N.J.); GIBCO BRL or Gibco BRL (Life Technologies, Inc., Gaithersburg, Md.); Millipore (Millipore, Billerica, Mass.); Bio-Rad (Bio-Rad, Hercules, Calif.); Invitrogen (Invitrogen Corp., San Diego, Calif.); NEB (New England Biolabs, Ipswich, Mass.); Sigma (Sigma Chemical Co., St. Louis, Mo.); Pierce (Pierce Biotechnology, Rockford, Ill.); Takara (Takara Bio Inc. Otsu, Japan); Roche (Hoffmann-La Roche, Basel, Switzerland); EM Science (EM Science, Gibbstown, N.J.); Qiagen (Qiagen, Inc., Valencia, Calif.); Biodesign (Biodesign Intl., Saco, Me.); Aptagen (Aptagen, Inc., Herndon, Va.); Sorvall (Sorvall brand, from Kendro Laboratory Products, Asheville, N.C.); United States Testing (United States Testing Co., Hoboken, N.J.); Molecular Devices (Molecular Devices, Corp., Sunnyvale, Calif.); R&D Systems (R&D Systems, Minneapolis, Minn.); Stratagene (Stratagene Cloning Systems, La Jolla, Calif.); Marsh (Marsh Biosciences, Rochester, N.Y.); Geneart (Geneart GmbH, Regensburg, Germany); DNA2.0 (DNA2.0, Menlo Park, Calif.); Gene Oracle (Gene Oracle, Mountain View, Calif.); Bio-Tek (Bio-Tek Instruments, Winooski, VT); Biacore (Biacore, Inc., Piscataway, N.J.); Woke (Woke, Leiden, The Netherlands); PeproTech (PeproTech, Rocky Hill, N.J.); SynPep (SynPep, Dublin, Calif.); New Objective (New Objective brand; Scientific Instrument Services, Inc., Ringoes, N.J.); Waters (Waters, Inc., Milford, Mass.); Matrix Science (Matrix Science, Boston, Mass.); Dionex (Dionex, Corp., Sunnyvale, Calif.); Monsanto (Monsanto Co., St. Louis, Mo.); Wintershall (Wintershall AG, Kassel, Germany); BASF (BASF Co., Florham Park, N.J.); Huntsman (Huntsman Petrochemical Corp., Salt Lake City, Utah); Enichem (Enichem Iberica, Barcelona, Spain); Fluka Chemie AG (Fluka Chemie AG, Buchs, Switzerland); Gist-Brocades (Gist-Brocades, NV, Delft, the Netherlands); Dow Corning (Dow Corning Corp., Midland, Mich.); and Microsoft (Microsoft, Inc., Redmond, Wash.).

Example 1 Assays

In the following Examples, various assays were used as set forth below for ease in reading. Any deviations from the protocols provided below are indicated in the Examples.

A. TCA Assay for Protein Content Determination in 96-well Microtiter Plates

For BPN′ (e.g., reference protease) and BPN′ variants, this assay was started using filtered culture supernatant from microliter plates grown 3-4 days at 33° C. with shaking at 230 rpm and humidified aeration. A fresh 96-well flat bottom microtiter plate (MTP) was used for the assay. First, 100 μL/well of 0.25 N HCl was placed in each well. Then, 50 μL of filtered culture broth was added. The light scattering/absorbance at 405 nm (use 5 sec mixing mode in the plate reader) was then determined, in order to provide the “blank” reading. For the test, 100 μL/well of 15% (w/v) trichloroacetic acid (TCA) was placed in the plates and incubated between 5 and 30 min at room temperature. The light scattering/absorbance at 405 nm (use 5 sec mixing mode in the plate reader) was then determined.

For GG36 (e.g., reference protease) and variants thereof, this assay was performed using filtered culture supernatant from microtiter plates grown approximately 3 days at 37° C. with shaking at 300 rpm and humidified aeration. In this assay 100 μL of a 0.25 M HCl solution was added to each well of a 96-well flat bottom microtiter plate. Subsequently, 25 μL aliquots of the filtered culture supernatants (containing the proteases) were added to wells. The light scattering/absorbance at 405 nm (using the 5 sec mixing mode in the plate reader) was then determined, in order to provide the “blank” reading. After this measurement, 100 μL of a 30% (w/v) TCA solution was added to each well and the microtiter plates were incubated between 5 and 15 minutes at room temperature. Finally, the resulting light scattering/absorbance at 405 nm (using the 5 sec mixing mode in the plate reader) was determined.

The equipment used was a Biomek FX Robot (Beckman Coulter) and a SpectraMAX (type 340; Molecular Devices) MTP Reader; the MTP's were from Costar (type 9017). The equipment used was a Biomek FX Robot (Beckman Coulter) and a SpectraMAX type 340 (Molecular Devices) MTP Reader; and the MTPs were type 9017 (Costar).

The calculations were performed by subtracting the blank (no TCA) from the test reading with TCA to provide a relative measure of the protein content in the samples. If desired, a standard curve can be created by calibrating the TCA readings with AAPF assays of clones with known conversion factors. However, the TCA results are linear with respect to protein concentration from 50 to 500 protein per ml (ppm) and can thus be plotted directly against enzyme performance for the purpose of choosing good-performing variants. The turbidity/light scatter increase in the samples correlates to the total amount of precipitable protein in the culture supernatant.

B. AAPF Protease Assay in 96-Well Microtiter Plates

In order to determine the protease activity of the proteases and variants thereof of the present invention, the hydrolysis of N-succinyl-L-alanyl-L-alanyl-L-prolyl-L-phenyl-p-nitroanilide (suc-AAPF-pNA) was measured. The reagent solutions used were: 100 mM Tris/HCl, pH 8.6, containing 0.005% TWEEN®-80 (Tris dilution buffer); 100 mM Tris buffer, pH 8.6, containing 10 mM CaCl₂ and 0.005% TWEEN®-80 (Tris/Ca buffer); and 160 mM suc-AAPF-pNA in DMSO (suc-AAPF-pNA stock solution) (Sigma: S-7388). To prepare a suc-AAPF-pNA working solution, 1 ml suc-AAPF-pNA stock solution was added to 100 ml Tris/Ca buffer and mixed well for at least 10 seconds. The assay was performed by adding 10 μl of diluted protease solution to each well, immediately followed by the addition of 190 μl 1 mg/ml suc-AAPF-pNA working solution. The solutions were mixed for 5 sec., and the absorbance change in kinetic mode (20 readings in 5 minutes) was read at 410 nm in an MTP reader, at 25° C. The protease activity was expressed as AU (activity=ΔOD·min⁻¹ ml⁻¹).

C. Surfactant and Chelant Stability Assays

LAS and LAS/EDTA stability was measured after incubation of the test protease in the presence of LAS and LAS/EDTA respectively, as a function of residual activity determined using the AAPF assay.

LAS Stability Method Reagents:

Dodecylbenzenesulfonate, Sodium salt (=LAS): Sigma D-2525

TWEEN®-80: Sigma P-8074

TRIS buffer (free acid): Sigma T-1378); 6.35 g is dissolved in about 960 ml water; pH is adjusted to 8.2 with 4N HCl. Final concentration of TRIS is 52.5 mM. LAS stock solution: Prepare a 10.5% LAS solution in MQ water (=10.5 g per 100 ml MQ) TRIS buffer-100 mM/pH 8.6 (100 mM Tris/0.005% Tween®-80) TRIS-Ca buffer, pH 8.6 (100 mM Tris/10 mM CaCl2/0.005% Tween-®80)

Hardware:

Flat bottom MTPs (Costar No. 9017)

Biomek FX ASYS Multipipettor Spectramax MTP Reader

iEMS Incubator/Shaker

Innova 4330 Incubator/Shaker

Biohit multichannel pipette

BMG Thermostar Shaker

A 0.063% LAS solution was prepared in 52.5 mM Tris buffer pH 8.2. The suc-AAPF-pNA working solution was prepared by adding 1 ml of 100 mg/ml suc-AAPF-pNA stock solution (in DMSO) to 100 ml (100 mM) TRIS buffer, pH 8.6. To dilute the supernatants, flat-bottomed plates were filled with dilution buffer and an aliquot of the supernatant was added and mixed well. The dilution ratio depended on the concentration of the protease controls in the growth plates (AAPF activity). The desired protein concentration was 80 ppm.

Ten μl of the diluted supernatant were added to 190 μl 0.063% LAS buffer/well. The MTP was covered with tape, shaken for a few seconds and placed in an incubator (Innova 4230) at 45° C. for BPN′ or GG36, for 60 minutes at 200 rpm agitation. The initial activity (t=10 minutes) was determined after 10 minutes of incubation by transferring 10 μl of the mixture in each well to a fresh MTP containing 190 μl suc-AAPF-pNA work solution. These solutions were mixed well and the AAPF activity was measured using a MTP Reader (20 readings in 5 minutes and 25° C.).

The final activity (t=60 minutes) was determined by removing another 10 μl of solution from the incubating plate after 60 minutes of incubation. The AAPF activity was then determined as described above. The stability of the samples was determined by calculating the ration of the residual and initial AAPF activity as follows:

Residual Activity (%)=[t−60 value]*100/[t−10 value].

LAS/EDTA Stability Method

The stability of protease variants in the presence of a representative anionic surfactant (LAS=linear alkylbene sulfonate, sodium dodecylbenzenesulfonate-DOBS) and di-sodium EDTA was measured after incubation under defined conditions and the residual activity was determined using the AAPF assay. The reagents used were dodecyllbenzene sulfonate, sodium salt (DOBS, Sigma No. D-2525), TWEEN®-80 (Sigma No. P-8074), di-sodium EDTA (Siegfried Handel No. 164599-02), HEPES (Sigma No. H-7523), unstress buffer: 50 mM HEPES (11.9 μl+0.005% TWEEN®-80, pH 8.0, Stress buffer: 50 mM HEPES (11.9 g/l), 0.1% (w/v) DOBS (1 g/l), 10 mM EDTA (3.36 g/l), pH 8.0, reference protease and protease variant culture supernatants, containing 200-400 μg/ml protein. The equipment used was V- or U-bottom MTP as dilution plates (Greiner 651101 and 650161 respectively), F-bottom MTP (Corning 9017) for unstress and LAS/EDTA buffer as well as for suc-AAPF-pNA plates, Biomek FX (Beckman Coulter), Spectramax Plus 384 MTP Reader (Molecular Devices), iEMS Incubator/Shaker (1 mm amplitude) (Thermo Electron Corporation), sealing tape: Nunc (236366)

The iEMS incubator/shaker (Thermo/Labsystems) was set at 29° C. Culture supernatants were diluted into plates containing unstress buffer to a concentration of ˜25 ppm (master dilution plate). 20 μl of sample from the master dilution plate was added to plates containing 180 μl unstress buffer to give a final incubation concentration of 2.5 ppm. The contents were mixed and kept at room temperature and a AAPF assay was performed on this plate. 20 μl of sample from the master dilution plate was also added to plates containing 180 μl stress buffer (50 mM HEPES (11.9 g/l), 0.1% (w/v) DOBS (1 g/l), 10 mM EDTA (3.36 g/l), pH 8.0). The solutions were mixed and immediately placed in 29° C. iEMS shaker for 30 min at 400 rpm. Following 30 minutes of incubation, a AAPF assay was performed on the stress plate. The stability of the samples was determined by calculating the ratio of the residual and initial AAPF activity as follows: Residual Activity (%)=[mOD.min−1 stressed]*100/[mOD. min−1 unstressed].

D. Cleaning Performance Assays

The stain removal performance of the protease variants was determined in commercially available detergents. Heat inactivation of commercial detergent formulas serves to destroy the enzymatic activity of any protein components while retaining the properties of non-enzymatic components. Thus this method was suitable for preparing commercially purchased detergents for use in testing the enzyme variants of the present invention.

Microswatches:

Microswatches of ¼″ circular diameter were obtained from CFT. Single microswatches or two microswatches were placed vertically in each well of a 96-well MTP to expose the whole surface area (i.e., not flat on the bottom of the well).

BMI Microswatch Assay

Microswatches containing blood milk and ink (BMI) of 0.25 inch circular diameter were obtained from CFT. Before cutting of the swatches, the fabric (EMPA 116) was washed with water. One microswatch was vertically placed in each well of a 96-well microliter plate in order to expose the whole surface area (i.e., not flat on the bottom of the well). The desired detergent solution was prepared as described herein. After equilibrating the Thermomixer at 25° C., 190 μl of detergent solution was added to each well of the MTP, containing microswatches. To this mixture, 10 μl of the diluted enzyme solution was added so that the final enzyme concentration was 1 ng/ml (determined from BCA assay). The MTP was sealed with tape and placed in the incubator for 30 minutes, with agitation at 1400 rpm. Following incubation under the appropriate conditions, 100 μl of the solution from each well was transferred into a fresh MTP. The new MTP containing 100 μl of solution/well was read at 405 nm using a MTP SpectraMax reader. Blank controls, as well as a control containing two microswatches and detergent but no enzyme were also included.

Baked Egg Microswatch Assay

The 96-well baked egg yolk substrate plates used in these assays were prepared from chicken egg yolks. Chicken egg yolks were separated from the whites, released from the membrane sac, and diluted 20% (vol/weight) with Milli-Q water. The diluted yolk was stirred for 15 min at room temperature using a magnetic stirrer. Five μL were carefully pipetted into the center of each well of a 96-well V-bottom plate (Costar #3894) using an 8-channel pipette. The plates were baked at 90° C. for 1 hour and cooled at room temperature. The baked egg yolk substrate plates were stored at room temperature and used within one week of preparation. Automatic dish detergents were prepared as described elsewhere in this document and pre-heated to 50° C. A 190 μL aliquot of detergent was added to each well of the 96-well plate using an 8-channel pipette. Ten μL of diluted enzyme was added to each well using a 96-channel pipetting device. The plate was carefully sealed with an adhesive foil sealer and incubated at 50° C. with shaking for 30 min. Then, 120 μL of the reaction mixture was transferred to a new 96-well flat-bottom plate, and the absorbance/light scattering was determined at 405 nm. The absorbance/light scattering at 405 nm is proportional to egg yolk removal.

Egg Yolk Microswatch Assay

Automatic dish detergents were prepared as described elsewhere in this document. The equipment used included a New Brunswick Innova 4230 shaker/incubator and a SpectraMAX (type 340) MTP reader. The MTPs were obtained from Costar (type 9017). Aged egg yolk with pigment swatches (CS-38) were obtained from Center for Test Materials. Before cutting 0.25-inch circular microswatches, the fabric was washed with water. One microswatch was placed in each well of a 96-well microliter plate. The test detergent was equilibrated at 50° C. 190 μl of detergent solution was added to each well of the MTP, containing microswatches. To this mixture, 10 μl of the diluted enzyme solution was added. The MTP was sealed with adhesive foil and placed in the incubator for 30 minutes, with agitation. Following incubation, 100 μl of the solution from each well was transferred into a fresh MTP. This MTP was read at 405 nm using a SpectraMax MTP reader. Blank controls, as well as controls containing microswatches and detergent but no enzyme were also included.

“3K” Swatch Fixation

This type of microswatch was pretreated using the fixation method described below. In a 10 liter beaker, 8 liters of distilled water were mixed well with 80 ml of 30% hydrogen peroxide using a ladle. Forty pieces of EMPA 116 swatches were laid down in a fan-type distribution prior to being added into the solution to ensure uniform fixation. Using the ladle, the swatches were swirled in the solution for a total of 30 minutes, continuously for the first five minutes and occasionally for the remaining 25 minutes. After the fixation process, the solution was discarded and the swatches were rinsed 6 times with approximately 6 liters of distilled water per rinse. After the rinse the swatches were put on top of paper towels to dry. The air-dried swatches were then punched using a ¼″ circular die on an expulsion press. Finally, a single microswatch was put into each well of a 96-well MTP vertically to expose the whole surface area (i.e. not flat on the bottom of the well).

“Pre-Washed” Swatch

This type of microswatch was pre-washed in deionised water for 20 minutes at ambient temperature. After the pre-washing step, the swatches were put on top of paper towels to dry. The air-dried swatches were then punched using a ¼″ circular die on an expulsion press. Finally two microswatches were put into each well of a 96-well MTP vertically to expose the whole surface area (i.e. not flat on the bottom of the well).

Detergents

For North American (NA) and Western European (WE) heavy duty liquid laundry (HDL) detergents, heat inactivation was performed by placing pre-weighed liquid detergent (in a glass bottle) in a water bath at 95° C. for 2 hours. The incubation time for heat inactivation of North American (NA) and Japanese (JPN) heavy duty granular laundry (HDG) detergent was 8 hours and that for Western European (WE) HDG detergent was 5 hours. The incubation time for heat inactivation of NA and WE auto dish washing (ADW) detergents was 8 hours. The detergents were purchased from local supermarket stores. Both un-heated and heated detergents were assayed within 5 minutes of dissolving the detergent to accurately determine percentage deactivated. Enzyme activity was tested by the AAPF assay.

Working solutions of detergents were made from the heat inactivated stocks. All of the detergents were commercially purchased detergents. Appropriate amounts of water hardness (6 gpg or 12 gpg) and buffer were added to the detergent solutions to match the desired conditions (Table 1-1). The solutions were mixed by vortexing or inverting the bottles.

TABLE 1-1 Laundry and Dish Washing Conditions Region Form Dose Detergent* Buffer Gpg pH T (° C.) Laundry (heavy duty liquid and granular) NA HDL 0.78 g/l   P&G TIDE ® 2X 5 mM HEPES 6 8.0 20 WE HDL 5.0 g/L Henkel Persil 5 mM HEPES 12 8.2 40 WE HDG 8.0 g/L P&G Ariel 2 mM Na₂CO₃ 12 10.5 40 JPN HDG 0.7 g/L P&G TIDE ® 2 mM Na₂CO₃ 6 10.0 20 NA HDG 1.0 g/L P&G TIDE ® 2 mM Na₂CO₃ 6 10.0 20 Automatic Dish Washing WE ADW 3.0 g/L RB Calgonit 2 mM Na₂CO₃ 21 10.0 40 NA ADW 3.0 g/L P&G Cascade 2 mM Na₂CO₃ 9 10.0 40 *Abbreviations: Procter & Gamble (P&G); and Reckitt Benckiser (RB).

The stain removal performance of reference serine proteases and variants therefrom on microswatches was determined on a MTP scale in commercially available detergent (Calgonit 5 int). The reagents used were: 5 mM HEPES, pH 8.0 or 5 mM MOPS, pH 7 buffer, 3:1 Ca:Mg for medium water hardness. (CaCl₂: MgCl2.6H2O); 15000 grains per gallon (gpg) stock diluted to 6 gpg, 2 BMI (blood/milk/ink) swatches per plate: EMPA-116 BMI cotton swatches processed by CFT: pre-rinsed and punched 2 swatches per well, and heat inactivated TIDE® 2× Cold off-the-shelf detergent in which lack of protease activity was confirmed.

TABLE 1-2 Working Detergent Solutions Temp Detergent Detergent (C.) g/L pH Buffer gpg Protease TIDE ® 2X Cold 16 0.98 8 5 mM 6 BPN′ HEPES TIDE ® 2X Cold 32 0.98 8 5 mM 6 GG36, HEPES BPN′ TIDE ® 2X Cold 16 0.98 7 5 mM 6 BPN′ MOPS

The incubator was set at the desired temperature (16° C. or 32° C.). 10 μL samples from the master dilution plate of ˜10 ppm enzyme was added to BMI 2-swatch plates with 190 μL working detergent solutions listed above. The volume was adjusted to give final concentration of 0.5 ppm for variants in the assay plates. The plates were immediately transferred to iEMS incubators and incubated for 30 minutes with 1400 rpm shaking at given temperature. Following incubation, 100 μL of supernatant was transferred into a new 96-well plate and the absorbance was measured in MTP Reader at 405 nm and/or 600 nm. Control wells, containing 1 or 2 microswatches and detergent without the addition of protease samples were also included in the test. The measurement at 405 nm provides a higher value and tracks pigment removal, while the measurement at 600 nm tracks turbidity and cleaning.

Calculation of the Stain Removal Activity for All Microswatch Assay Methods:

The absorbance value obtained was corrected for the blank value (substrate without enzyme), providing a measure of hydrolytic activity. For each sample (variant) the performance index was calculated. The performance index compares the performance of the variant (actual value) and the standard enzyme (theoretical value) at the same protein concentration. In addition, the theoretical values can be calculated, using the parameters of the Langmuir equation of the standard enzyme.

Enzymes and Equipment

Samples of reference serine proteases variants thereof were obtained from filtered culture broth of cultures grown in MTP plates. The equipment used was a Biomek FX Robot (Beckman Coulter), a SpectraMAX MTP Reader (type 340; Molecular Devices), an iEMS incubator/shaker (Thermo/Labsystems); F-bottom MTPs (Costar type 9017 used for reading reaction plates after incubation); and V-bottom MTPs (Greiner 651101 used for pre-dilution of supernatant). In this assay, the proteases hydrolyze the substrate and liberate pigment and insoluble particles from the substrate. Thus the rate of turbidity is a measure of enzyme activity.

E. Relative Specific Activity of Proteases and Variants Thereof

In order to discriminate the protease variants, the apparent relative specific activity was calculated using suc-AAPF-pNA as a substrate, which enabled the comparison and ranking of the variants versus the wild-type or standard protease. The specific activity on the suc-AAPF-pNA substrate was determined by dividing the proteolytic activity by the measured TCA-values of each sample, using the assays described above. Using these values, the relative specific activity was calculated (specific activity of variant/specific activity of reference protease).

F. Dishwashing Performance

The performance of the protease variants was tested under various automatic dishwashing conditions. The compositions of the dish detergents are shown in the following Tables. These detergents are commercially available from wfk Testmaterials (www.testgewebe.de/en/products/detergents/) and are referred to by their wfk Testmaterials designations. These detergents were obtained from the source without the presence of enzymes, to permit analysis of the protease variants.

TABLE 1-3 Phosphate-Free Detergent IEC-60436 WFK Type B (pH = 10.4 in 3 g/l) Component Wt % Sodium citrate dehydrate 30.0 Maleic acid/Acrylic acid copolymer sodium Salt 12.0 Sodium perborate monohydrate 5.0 TAED 2.0 Sodium disilicate: Protil A (Cognis) 25.0 Linear fatty alcohol ethoxylate 2.0 Sodium carbonate anhydrous add to 100

TABLE 1-4 Phosphate-Containing Detergent: IEC- 60436 WFK Type C (pH = 10.5 in 3 g/l) Component Wt % Sodium tripolyphosphate 23.0 Sodium citrate dehydrate 22.3 Maleic acid/Acrylic acid copolymer sodium salt 4.0 Sodium perborate monohydrate 6.0 TAED 2.0 Sodium disilicate: Protil A (Cognis) 5.0 Linear fatty alcohol ethoxylate 2.0 Sodium carbonate anhydrous add to 100

The protocols for preparation of each of the stain types (egg yolk, minced meat and egg, and egg with milk) are provided below. Before the individual soil types were applied to the test dishes, the dishes were thoroughly washed. This was particularly necessary, as residues of certain persistent stains may still be present on the dishes from previous tests. New dishes were also subjected to three thorough washes before being used for the first time in a test.

Preparation of Egg Yolk Stains on Stainless Steel

The stainless steel sheets (10×15 cm; brushed on one side) used in these experiments were thoroughly washed at 95° C. in a laboratory dishwasher with a high-alkalinity commercial detergent (e.g., ECOLAB® detergent; Henkel) to provide sheets that were clean and grease-free. These sheets were deburred prior to their first use. The sheets were dried for 30 minutes at 80° C. in a thermal cabinet before being soiled with egg yolk. The surfaces to be brushed were not touched prior to soiling. Also, no water stains or fluff on the surfaces were permitted. The cooled sheets were weighed before soiling.

The egg yolks were prepared by separating the yolks of approximately 10-11 eggs (200 g of egg yolk) from the whites. The yolks were stirred with a fork in a glass beaker to homogenize the yolk suspension. The yolks were then strained (approximately 0.5 mm mesh) to remove coarse particles and any egg shell fragments.

A flat brush (2.5″) was used to apply 2.0±0.1 g egg yolk suspension as uniformly as possible over an area of 140 cm² on the brushed sides of each of the stainless steel sheets, leaving an approximately 1 cm wide unsoiled rim (adhesive tape was used if needed). The soiled sheets were dried horizontally (to prevent formation of droplets on the edges of the sheets), at room temperature for 4 hours (max. 24 hr).

To denaturate the egg yolk proteins, the sheets were immersed for 30 seconds in boiling, demineralized water (using a holding device if necessary). Then the sheets were dried again for 30 min at 80° C. After drying and cooling, the sheets were weighed. After weighing, the sheets were left for at least 24 hrs (20° C., 40-60% relatively humidity) before submitting them to the wash test. In order to meet the testing requirements, only sheets with 1000±100 mg/140 cm² (egg yolk after denaturation) were used in the testing. After the wash tests were conducted, the sheets were dried for 30 min at 80° C. in the thermal cabinet and weighed again after cooling. The percent cleaning performance was determined by dividing the mg of egg yolk released upon washing by the mg of denatured egg yolk applied and multiplying by 100.

Preparation of Minced Meat and Egg Stains on Porcelain Plates

For these experiments, dessert plates (Arzberg, 19 cm diameter, white, glazed porcelain) conforming to EN 50242, form 1495, No. 0219, were used. A total of 225 g lean pork and beef (50:50 ratio) was finely chopped and maintained cool. The mixture was twice run through a mincer. Temperatures above 35° C. were avoided. The 225 g of the minced meat was then mixed with 75 g of egg (white and yolk mixed together). The preparation was then frozen for up to three months at −18° C., prior to use. If pork was not available, 100% beef was used, as these are interchangeable.

The minced meat and egg mixture (300 g) was brought to room temperature and mixed with 80 ml demineralized water. The mixture was then homogenized for 2 min using a kitchen hand blender. A fork was used to spread 3 g of the minced meat/egg/water mixture on each white porcelain plate, leaving an approximately 2 cm wide unsoiled margin around the rim. The amount applied was 11.8±0.5 mg/cm². The plates were dried for 2 hours at 120° C. in a preheated thermal cabinet. As soon as the plates were cooled, they were ready for use.

After conducting the dishwashing tests, the plates were sprayed with ninhydrin solution (prepared to 1% in ethanol) for better identification of the minced meat protein residues. To promote the color reaction, the plates were heated for 10 min at 80° C. in the thermal cabinet. Evaluation of the washing performance was done by visually inspecting the color reactions of the minced meat residue with reference to the IKW photographic catalogue (IKW—The German Cosmetic, Toiletry, Perfumery and Detergent Association).

Preparation of Egg/Milk Stains on Stainless Steel

The stainless steel sheets (10×15 cm; brushed on one side) used in these experiments were thoroughly washed at 95° C. in a laboratory dishwasher with a high-alkalinity commercial detergent to remove grease and clean the sheets. The sheets were polished dry with a cellulose cloth. The surfaces to be brushed were not touched prior to soiling. Also, no water stains or fluff on the surfaces were permitted. Before soiling, the sheets were placed in a thermal cabinet at 80° C., for 30 min. The cooled sheets were weighed before soiling.

The egg yolks and whites of whole raw eggs (3-4 eggs; approximately 160 g/egg) were placed in a bowl and beaten with an egg whisk. Then, 50 ml semi-skimmed milk (1.5% fat, ultra-high-temperature, homogenized) were added to the mixture. The milk and egg were mixed without generating froth. A flat brush was used to uniformly distribute 1.0±0.1 g of the egg/milk mixture on the brushed side of the stainless steel sheets, using a balance to check the distribution. A margin of approximately 1.0 cm was left around the short sides of the sheets. The soiled sheets were dried horizontally (to prevent formation of droplets on the edges of the sheets), at room temperature for 4 hours (max. 24 hr).

The sheets were then immersed for 30 seconds in boiling, demineralized water (using a holding device if necessary). Then the sheets were dried again for 30 min at 80° C. After drying and cooling the sheets were weighed. After weighing the sheets were left to sit for at least 24 hours (20° C., 40-60% relatively humidity) before submitting them to the wash test. In order to meet the testing requirements, only sheets with 190±10 mg egg yolk/milk were used.

After the wash tests were conducted, the sheets were dried for 30 min at 80° C., in the thermal cabinet, and weighed again after cooling. The percentage cleaning performance was determined by dividing the mg of egg/milk released upon washing by the mg of egg/milk applied and multiplying by 100.

Washing Equipment and Conditions

The washing tests were performed in an automatic dishwasher (Miele model G690SC), equipped with soiled dishes and stainless steel sheets, prepared as described above. A defined amount of the detergent was used. The temperature tested was 50° C. The water hardness was 21° GH (German hardness). As described above, after washing the plates soiled with minced meat were visually assessed using a photo rating scale of 0 to 10, wherein “0” designated a completely dirty plate and “10” designated a clean plate. These values correspond to the stain or soil removal (SR) capability of the enzyme-containing detergent. The washed stainless steel plates soiled with egg yolk or egg yolk/milk were analyzed gravimetrically to determine the amount of residual stain after washing. The variant proteases were tested at a level of between 0 and 30 mg/active protein per wash.

G. Eglin C Inhibition Assay

As described herein, serine protease concentration and specific activity was determined by titration with an inhibitor. Eglin c from the leech Hirudo medicinalis is a tight-binding protein inhibitor of subtilisins and ASP protease (Heinz et al., Biochemistry, 31: 8755-66, 1992), and can therefore be used to measure enzyme concentration, which in turn permits specific activity to be calculated. Briefly, one measures the amount of enzyme inhibition produced by several known concentrations of eglin c. From this information, the concentration of eglin c required for complete inhibition is calculated. This is equivalent to the enzyme concentration in the sample.

Protease activity was measured using the chromogenic AAPF assay described above. The gene for eglin c was synthesized and expressed in E. coli by standard methods. Its properties and inhibitory potency were the same as eglin c purchased from Sigma. The concentration of an eglin c stock solution was determined by measuring the inhibition of a sample of Bacillus lentus subtilisin of known specific activity. Then the calibrated eglin c sample was used to determine the concentration and specific activity of subtilisin variants. These values were used to create normalized 96-well enzyme stock plates, where all of the variants were diluted to a common concentration.

H. Performance Index

The performance index compares the performance of the variant (actual value) and the standard or reference protease (theoretical value) at the same protein concentration. In addition, the theoretical values can be calculated, using the parameters of the binding curve (i.e., Langmuir equation) of the standard protease. A performance index (PI) that is greater than 1 (PI>1) identifies a better variant as compared to the standard (e.g., wild-type), while a PI of 1 (PI=1) identifies a variant that performs the same as the standard, and a PI that is less than 1 (PRO identifies a variant that performs worse than the standard. Thus, the PI identifies winners, as well as variants that are less desirable for use under certain circumstances.

Example 2 Production of BPN′ Protease in B. subtilis

In this Example, experiments conducted to produce BPN′ protease in B. subtilis, are described. Transformation of plasmid pHPLT-BPN′ into B. subtilis was performed as known in the art (See e.g., WO 02/14490, incorporated herein by reference). The DNA sequence (aprE-BPN′ hybrid leader, BPN′ pro and BPN′ mature DNA sequence from B. amyloliquefaciens) provided below, encodes the BPN′ precursor protein:

(SEQ ID NO: 1) GTGAGAAGCAAAAAATTGTGGATCAGTTTGCTGTTTGCTTTAGCGTTA ATCTTTACGATGGCGTTCGGCAGCACATCCTCTGCCCAGGCGGCAGGG AAATCAAACGGGGAAAAGAAATATATTGTCGGGTTTAAACAGACAATG AGCACGATGAGCGCCGCTAAGAAGAAAGATGTCATTTCTGAAAAAGGC GGGAAAGTGCAAAAGCAATTCAAATATGTAGACGCAGCTTCAGCTACA TTAAACGAAAAAGCTGTAAAAGAATTGAAAAAAGACCCGAGCGTCGCT TACGTTGAAGAAGATCACGTAGCACATGCGTAC GCGCAGTCCGTGCCT TACGGCGTATCACAAATTAAAGCCCCTGCTCTGCACTCTCAAGGCTAC ACTGGATCAAATGTTAAAGTAGCGGTTATCGACAGCGGTATCGATTCT TCTCATCCTGATTTAAAGGTAGCAGGCGGAGCCAGCATGGTTCCTTCT GAAACAAATCCTTTCCAAGACAACAACTCTCACGGAACTCACGTTGCC GGCACAGTTGCGGCTCTTAATAACTCAATCGGTGTATTAGGCGTTGCG CCAAGCGCATCACTTTACGCTGTAAAAGTTCTCGGTGCTGACGGTTCC GGCCAATACAGCTGGATCATTAACGGAATCGAGTGGGCGATCGCAAAC AATATGGACGTTATTAACATGAGCCTCGGCGGACCTTCTGGTTCTGCT GCTTTAAAAGCGGCAGTTGATAAAGCCGTTGCATCCGGCGTCGTAGTC GTTGCGGCAGCCGGTAACGAAGGCACTTCCGGCAGCTCAAGCACAGTG GGCTACCCTGGTAAATACCCTTCTGTCATTGCAGTAGGCGCTGTTGAC AGCAGCAACCAAAGAGCATCTTTCTCAAGCGTAGGACCTGAGCTTGAT GTCATGGCACCTGGCGTATCTATCCAAAGCACGCTTCCTGGAAACAAA TACGGGGCGTACAACGGTACGTCAATGGCATCTCCGCACGTTGCCGGA GCGGCTGCTTTGATTCTTTCTAAGCACCCGAACTGGACAAACACTCAA GTCCGCAGCAGTTTAGAAAACACCACTACAAAACTTGGTGATTCTTTC TACTATGGAAAAGGGCTGATCAACGTACAGGCGGCAGCTCAGTAA.

In the above sequence, bold indicates the DNA that encodes the mature protease, standard font indicates the leader sequence (aprE-BPN′ hybrid leader), and the underlined indicates the pro sequences (BPN′). The amino acid sequence (aprE-BPN′ hybrid leader, BPN′ pro and BPN′ mature DNA sequence) of the BPN′ precursor protein is provided below. In this sequence, bold and underlined indicates the mature BPN′ protease.

(SEQ ID NO: 2) VRSKKLWISLLFALALIFTMAFGSTSSAQAAGKSNGEKKYIVGFKQTM STMSAAKKKDVISEKGGKVQKQFKYVDAASATLNEKAVKELKKDPSVA YVEEDHVAHAY AQSVPYGVSQIKAPALHSQGYTGSNVKVAVIDSGIDS SHPDLKVAGGASMVPSETNPFQDNNSHGTHVAGTVAALNNSIGVLGVA PSASLYAVKVLGADGSGQYSWIINGIEWAIANNMDVINMSLGGPSGSA ALKAAVDKAVASGVVVVAAAGNEGTSGSSSTVGYPGKYPSVIAVGAVD SSNQRASFSSVGPELDVMAPGVSIQSTLPGNKYGAYNGTSMASPHVAG AAALILSKHPNWTNTQVRSSLENTTTKLGDSFYYGKGLINVQAAAQ Construction of BPN′ Expression Vector (pHPLT-BPN′)

PCR fragments were obtained using standard conditions with TGO polymerase (Roche Diagnostics) using pJH101term. Plasmid pJH101 corresponds to pJH101 (Ferrari et al., J Bacteriol, 154:1513-5 [1983]) with the following fragment inserted in the EcoRI/BamHI site:

(SEQ ID NO: 3) GAATTCCTCCATTTTCTTCTGCTATCAAAATAACAGACTCGTGATTTT CCAAACGAGCTTTCAAAAAAGCCTCTGCCCCTTGCAAATCGGATGCCT GTCTATAAAATTCCCGATATTGGCTTAAACAGCGGCGCAATGGCGGCC GCATCTGATGTCTTTGCTTGGCGAATGTTCATCTTATTTCTTCCTCCC TCTCAATAATTTTTTCATTCTATCCCTTTTCTGTAAAGTTTATTTTTC AGAATACTTTTATCATCATGCTTTGAAAAAATATCACGATAATATCCA TTGTTCTCACGGAAGCACACGCAGGTCATTTGAACGAATTTTTTCGAC AGGAATTTGCCGGGACTCAGGAGCATTTAACCTAAAAAAGCATGACAT TTCAGCATAATGAACATTTACTCATGTCTATTTTCGTTCTTTTCTGTA TGAAAATAGTTATTTCGAGTCTCTACGGAAATAGCGAGAGATGATATA CCTAAATAGAGATAAAATCATCTCAAAAAAATGGGTCTACTAAAATAT TATTCCATCTATTACAATAAATTCACAGAATAGTCTTTTAAGTAAGTC TACTCTGAATTTTTTTAAAAGGAGAGGGTAAAGAGTGAGAAGCAAAAA ATTGTGGATCAGTTTGCTGTTTGCTTTAGCGTTAATCTTTACGATGGC GTTCGGCAGCACATCCTCTGCCCAGGCGGCAGGGAAATCAAACGGGGA AAAGAAATATATTGTCGGGTTTAAACAGACAATGAGCACGATGAGCGC CGCTAAGAAGAAAGATGTCATTTCTGAAAAAGGCGGGAAAGTGCAAAA GCAATTCAAATATGTAGACGCAGCTTCAGCTACATTAAACGAAAAAGC TGTAAAAGAATTGAAAAAAGACCCGAGCGTCGCTTACGTTGAAGAAGA TCACGTAGCACATGCGTACGCGCAGTCCGTGCCTTACGGCGTATCACA AATTAAAGCCCCTGCTCTGCACTCTCAAGGCTACACTGGATCAAATGT TAAAGTAGCGGTTATCGACAGCGGTATCGATTCTTCTCATCCTGATTT AAAGGTAGCAGGCGGAGCCAGCATGGTTCCTTCTGAAACAAATCCTTT CCAAGACAACAACTCTCACGGAACTCACGTTGCCGGCACAGTTGCGGC TCTTAATAACTCAATCGGTGTATTAGGCGTTGCGCCAAGCGCATCACT TTACGCTGTAAAAGTTCTCGGTGCTGACGGTTCCGGCCAATACAGCTG GATCATTAACGGAATCGAGTGGGCGATCGCAAACAATATGGACGTTAT TAACATGAGCCTCGGCGGACCTTCTGGTTCTGCTGCTTTAAAAGCGGC AGTTGATAAAGCCGTTGCATCCGGCGTCGTAGTCGTTGCGGCAGCCGG TAACGAAGGCACTTCCGGCAGCTCAAGCACAGTGGGCTACCCTGGTAA ATACCCTTCTGTCATTGCAGTAGGCGCTGTTGACAGCAGCAACCAAAG AGCATCTTTCTCAAGCGTAGGACCTGAGCTTGATGTCATGGCACCTGG CGTATCTATCCAAAGCACGCTTCCTGGAAACAAATACGGGGCGTACAA CGGTACGTCAATGGCATCTCCGCACGTTGCCGGAGCGGCTGCTTTGAT TCTTTCTAAGCACCCGAACTGGACAAACACTCAAGTCCGCAGCAGTTT AGAAAACACCACTACAAAACTTGGTGATTCTTTCTACTATGGAAAAGG GCTGATCAACGTACAGGCGGCAGCTCAGTAAAACATAAAAAACCGGCC TTGGCCCCGCCGGTTTTTTATTATTTTTCTTCCTCCGCATGTTCAATC CGCTCCATAATCGACGGATGGCTCCCTCTGAAAATTTTAACGAGAAAC GGCGGGTTGACCCGGCTCAGTCCCGTAACGGCCAAGTCCTGAAACGTC TCAATCGCCGCTTCCCGGTTTCCGGTCAGCTCAATGCCGTAACGGTCG GCGGCGTTTTCCTGATACCGGGAGACGGCATTCGTAATCGGATCC.

This fragment contains the BPN′ gene with a fusion signal sequence (containing the first eight amino acids of the aprE signal sequence of B. subtilis followed by the BPN′ signal sequence of B. amyloliquefaciens starting at the 9th amino acid). This fragment was used as a template for a PCR reaction employing the following primers: AK04-14: GtcctctgttaacTTACTGAGCTGCCGCCTGTAC (SEQ ID NO:4) annealing to the 3′ end of the BPN′ mature gene, introducing a HpaI site downstream of the translational stop codon; and AK04-21.1: TTATGCGAGgctagcaaaaggagagggtaaagagtgagaagc (SEQ ID NO:5) annealing to the 5′ end of the BPN′ signal sequence introducing a NheI site at the 5′ end. [01] The PCR fragment obtained from this reaction was cleaned over a Qiagen PCR cleaning kit using standard conditions. After digesting the cleaned fragment with the restriction enzymes NheI and HpaI under standard conditions, it was ligated into a NheI/HpaI digested vector containing the LAT promoter (pHPLT-VAAc1, described in US2006/0014265 and See FIG. 3A).

Subsequently, the pHPLT-BPN′ ligation mixture was transformed into B. subtilis (ΔaprE, ΔnprE, oppA, ΔspoIIE, degUHy32, ΔamyE::(xylR,pxylA-comK) as described in WO 02/14490, incorporated herein by reference. Selective growth of B. subtilis transformants harboring the pHPLT-BPN′ vector (See, FIG. 3B) was performed in shake flasks containing 25 ml MBD medium (a MOPS based defined medium), with 20 mg/L neomycin. Incubation of the transformed cells resulted in the production of secreted BPN′ protease having proteolytic activity. Gel analysis was performed using NuPage Novex 10% Bis-Tris gels (Invitrogen®, Catalog No. NP0301BOX). To prepare samples for analysis, 2 volumes of supernatant were mixed with 1 volume 1M HCl, 1 volume 4×LDS sample buffer (Invitrogen®, Catalog No. NP0007), and 1% PMSF (20 mg/ml), and subsequently heated for 10 minutes at 70° C. Then, 25 μL of each sample was loaded onto the gel, together with 10 μL of SeeBlue plus 2 pre-stained protein standards (Invitrogen®, Catalog No. LC5925). The results clearly demonstrated that the BPN′ cloning strategy described in this Example yielded active BPN′ produced by B. subtilis.

Example 3 Generation of BPN′ Site Evaluation Libraries and Multiple Mutation Libraries

In this Example, the construction of BPN′ variants is described.

BPN′ Site Evaluation Library (SEL) Construction

The pHPLT-BPN′ vector containing the BPN′ expression cassette served as template DNA. This vector contains a unique BglII restriction site, which was utilized in SEL construction. Primers synthesized by Invitrogen® (desalted, 50 nmol scale) and listed in Table 7-1, were used to generate the libraries.

To construct BPN′ SELs, three PCR amplifications were performed: two mutagenesis PCRs to introduce the mutated codon of interest in the mature BPN′ DNA sequence and a third PCR to fuse the two mutagenesis PCRs in order to construct the pHPLT-BPN′ expression vector having the desired mutated codon in the mature BPN′ sequence. The method of mutagenesis was based on the codon-specific mutation approach. In this method, the creation of all possible mutations at a time in a specific DNA triplet is performed using forward and reverse oligonucleotide primers with a length of 25 to 45 nucleotides enclosing a specific designed triple DNA sequence (NNS with N=A, C, T or G, and S=C or G) that corresponds with the sequence of the codon to be mutated. This guarantees random incorporation of nucleotides at that specific BPN′ mature codon. The number listed in the primer name (Table 3-1) corresponds with the specific BPN′ mature codon position. Two additional primers that were used to construct the SELs contained a BglII restriction site together with a portion of the pHPLT-BPN′DNA sequence flanking the BglII restriction site.

Construction of each SEL began with two primary PCR amplifications using the pHPLT-BglII-FW primer and a specific BPN′ reverse mutagenesis primer, and for the second PCR amplification the pHPLT-BglII-RV primer and a specific BPN′ forward mutagenesis primer (equal BPN′ mature codon positions for the forward and reverse mutagenesis primers). The introduction of the mutations in the mature BPN′ sequence was performed using Finnzymes Phusion High-Fidelity DNA Polymerase (Catalog No. F-530L). All PCR amplifications were executed according to Finnzymes protocol supplied with the polymerase. The PCR conditions were as follows:

For primary PCR 1:

pHPLT-BglII-FW primer and a specific BPN′ reverse mutagenesis primer - both 1 μL (10 μM); and for primary PCR 2: pHPLT-BglII-RV primer and a specific BPN′ forward mutagenesis primer - both 1 μL (10 (μM); in 5X Phusion HF buffer 10 μL  10 mM dNTP mixture 1 μL Phusion DNA polymerase 0.75 μL (2 units/μL) DMSO, 100% 1 μL pHPLT-BPN′ template DNA 1 μL (0.1-1 ng/μL) Distilled, autoclaved water up to 50 μL

PCR was completed using a MJ Research (Location) PTC-200 Peltier thermal cycler with the following PCR program: 30 seconds 98° C., 30× (10 seconds 98° C., 20 seconds 55° C., 1 minute 72° C.) and 5 min 72° C. The reactions resulted in two fragments of approximately 2 to 3 kB in length, which had about 30 nucleotide base overlap around the BPN′ mature codon of interest. Fragments were fused in a third reaction using the two aforementioned fragments and the forward and reverse BglII primers. The fusion PCR reaction was carried out as follows:

pHPLT-BglII-FW primer and pHPLT-BglII-RV primer - both 1 μL (10 μM) 5X Phusion HF buffer 10 μL  10 mM dNTP mixture 1 μL Phusion DNA polymares 0.75 μL (2 units/μL) DMSO, 100% 1 μL primary PCR 1 reaction mix 1 μL primary PCR 2 reaction mix 1 μL Distilled, autoclaved water up to 50 μL

The PCR fusion program was as follows: 30 seconds 98° C., 30× (10 seconds 98° C., 20 seconds 55° C., 2:05 minute 72° C.) and 5 min 72° C. using a MJ Research® PTC-200 Peltier thermal cycler.

The amplified linear 4.8 Kb fragment was purified using the Qiagen® Qiaquick PCR purification kit (Catalog No. 28106) and digested with the BglII restriction enzyme to create cohesive ends on both sides of the fusion fragment. The digestion reactions contained:

35 μL purified linear DNA fragment

4 μL React® 3 buffer (Invitrogen®)

1 μL BglII, 10 units/ml (Invitrogen®)

Reaction conditions: 1 hour, 30° C.

Ligation of the BglII digested and purified fragment yielded circular and multimeric DNA products containing the desired mutation, which were subsequently directly transformed into competent Bacillus subtilis:

30 μL of purified BglII digested DNA fragment

8 μL T4 DNA Ligase buffer (Invitrogen® Catalog No. 46300-018)

1 μL T4 DNA Ligase, 1 unit/μL, (Invitrogen® Catalog No. 15224-017)

Reaction conditions: 16-20 hours, 16° C.

The ligation mixture was used to transform B. subtilis (ΔaprE, ΔnprE, oppA, ΔspoIIE, degUHy32, ΔamyE::(xylR,pxylA-comK) as described in WO 02/14490, incorporated herein by reference. For each library, 96 single colonies were picked and grown in MOPS media containing neomycin and 1.25 g/L yeast extract, for sequence analysis (BaseClear) and screening purposes. The library numbers ranged from 1 to 275. Each number represents the codon of the mature bpn′ sequence that was randomly mutated. Each library contained a maximum of 19 BPN′ variants.

TABLE 3-1 BPN′ Primers SEQ Primer ID Name Oligonucleotide Sequence NO: pHPLT-BPN BglII containing primers pHPLT- GCAATCAGATCTTCCTTCAGGTTATGACC 6 BgLII-FW pHPLT- GCATCGAAGATCTGATTGCTTAACTGCTTC 7 BglII-RV BPN′ Mutagenesis Primers (F = Forward and R = Reverse) BPN1F CACGTAGCACATGCATACNNSCAGTCCGTGCCTTAC 8 GGC BPN2F GTAGCACATGCATACGCGNNSTCCGTGCCTTACGGC 9 GTA BPN3F GCACATGCATACGCGCAGNNSGTGCCTTACGGCGTA 10 TCA BPN4F CATGCATACGCGCAGTCCNNSCCTTACGGCGTATCA 11 CAA BPN5F GCATACGCGCAGTCCGTGNNSTACGGCGTATCACAA 12 ATT BPN6F TACGCGCAGTCCGTGCCTNNSGGCGTATCACAAATT 13 AAA BPN7F GCGCAGTCCGTGCCTTACNNSGTATCACAAATTAAA 14 GCC BPN8F CAGTCCGTGCCTTACGGCNNSTCACAAATTAAAGCC 15 CCT BPN9F TCCGTGCCTTACGGCGTANNSCAAATTAAAGCCCCT 16 GCT BPN10F GTGCCTTACGGCGTATCANNSATTAAAGCCCCTGCT 17 CTG BPN11F CCTTACGGCGTATCACAANNSAAAGCCCCTGCTCTG 18 CAC BPN12F TACGGCGTATCACAAATTNNSGCCCCTGCTCTGCAC 19 TCT BPN13F GGCGTATCACAAATTAAANNSCCTGCTCTGCACTCT 20 CAA BPN14F GTATCACAAATTAAAGCCNNSGCTCTGCACTCTCAA 21 GGC BPN15F TCACAAATTAAAGCCCCTNNSCTGCACTCTCAAGGC 22 TAC BPN16F CAAATTAAAGCCCCTGCTNNSCACTCTCAAGGCTAC 23 ACT BPN17F ATTAAAGCCCCTGCTCTGNNSTCTCAAGGCTACACT 24 GGA BPN18F AAAGCCCCTGCTCTGCACNNSCAAGGCTACACTGGA 25 TCA BPN19F GCCCCTGCTCTGCACTCTNNSGGCTACACTGGATCA 26 AAT BPN20F CCTGCTCTGCACTCTCAANNSTACACTGGATCAAAT 27 GTT BPN21F GCTCTGCACTCTCAAGGCNNSACTGGATCAAATGTT 28 AAA BPN22F CTGCACTCTCAAGGCTACNNSGGATCAAATGTTAAA 29 GTA BPN23F CACTCTCAAGGCTACACTNNSTCAAATGTTAAAGTA 30 GCG BPN24F TCTCAAGGCTACACTGGANNSAATGTTAAAGTAGCG 31 GTT BPN25F CAAGGCTACACTGGATCANNSGTTAAAGTAGCGGTT 32 ATC BPN26F GGCTACACTGGATCAAATNNSAAAGTAGCGGTTATC 33 GAC BPN27F TACACTGGATCAAATGTTNNSGTAGCGGTTATCGAC 34 AGC BPN28F ACTGGATCAAATGTTAAANNSGCGGTTATCGACAGC 35 GGT BPN29F GGATCAAATGTTAAAGTANNSGTTATCGACAGCGGT 36 ATC BPN30F TCAAATGTTAAAGTAGCGNNSATCGACAGCGGTATC 37 GAT BPN31F AATGTTAAAGTAGCGGTTNNSGACAGCGGTATCGAT 38 TCT BPN32F GTTAAAGTAGCGGTTATCNNSAGCGGTATCGATTCT 39 TCT BPN33F AAAGTAGCGGTTATCGACNNSGGTATCGATTCTTCT 40 CAT BPN34F GTAGCGGTTATCGACAGCNNSATCGATTCTTCTCAT 41 CCT BPN35F GCGGTTATCGACAGCGGTNNSGATTCTTCTCATCCT 42 GAT BPN36F GTTATCGACAGCGGTATCNNSTCTTCTCATCCTGAT 43 TTA BPN37F ATCGACAGCGGTATCGATNNSTCTCATCCTGATTTA 44 AAG BPN38F GACAGCGGTATCGATTCTNNSCATCCTGATTTAAAG 45 GTA BPN39F AGCGGTATCGATTCTTCTNNSCCTGATTTAAAGGTA 46 GCA BPN40F GGTATCGATTCTTCTCATNNSGATTTAAAGGTAGCA 47 GGC BPN41F ATCGATTCTTCTCATCCTNNSTTAAAGGTAGCAGGC 48 GGA BPN42F GATTCTTCTCATCCTGATNNSAAGGTAGCAGGCGGA 49 GCC BPN43F TCTTCTCATCCTGATTTANNSGTAGCAGGCGGAGCC 50 AGC BPN44F TCTCATCCTGATTTAAAGNNSGCAGGCGGAGCCAGC 51 ATG BPN45F CATCCTGATTTAAAGGTANNSGGCGGAGCCAGCATG 52 GTT BPN46F CCTGATTTAAAGGTAGCANNSGGAGCCAGCATGGTT 53 CCT BPN47F GATTTAAAGGTAGCAGGCNNSGCCAGCATGGTTCCT 54 TCT BPN48F TTAAAGGTAGCAGGCGGANNSAGCATGGTTCCTTCT 55 GAA BPN49F AAGGTAGCAGGCGGAGCCNNSATGGTTCCTTCTGAA 56 ACA BPN50F GTAGCAGGCGGAGCCAGCNNSGTTCCTTCTGAAACA 57 AAT BPN51F GCAGGCGGAGCCAGCATGNNSCCTTCTGAAACAAAT 58 CCT BPN52F GGCGGAGCCAGCATGGTTNNSTCTGAAACAAATCCT 59 TTC BPN53F GGAGCCAGCATGGTTCCTNNSGAAACAAATCCTTTC 60 CAA BPN54F GCCAGCATGGTTCCTTCTNNSACAAATCCTTTCCAA 61 GAC BPN55F AGCATGGTTCCTTCTGAANNSAATCCTTTCCAAGAC 62 AAC BPN56F ATGGTTCCTTCTGAAACANNSCCTTTCCAAGACAAC 63 AAC BPN57F GTTCCTTCTGAAACAAATNNSTTCCAAGACAACAAC 64 TCT BPN58F CCTTCTGAAACAAATCCTNNSCAAGACAACAACTCT 65 CAC BPN59F TCTGAAACAAATCCTTTCNNSGACAACAACTCTCAC 66 GGA BPN60F GAAACAAATCCTTTCCAANNSAACAACTCTCACGGA 67 ACT BPN61F ACAAATCCTTTCCAAGACNNSAACTCTCACGGAACT 68 CAC BPN62F AATCCTTTCCAAGACAACNNSTCTCACGGAACTCAC 69 GTT BPN63F CCTTTCCAAGACAACAACNNSCACGGAACTCACGTT 70 GCC BPN64F TTCCAAGACAACAACTCTNNSGGAACTCACGTTGCC 71 GGC BPN65F CAAGACAACAACTCTCACNNSACTCACGTTGCCGGC 72 ACA BPN66F GACAACAACTCTCACGGANNSCACGTTGCCGGCACA 73 GTT BPN67F AACAACTCTCACGGAACTNNSGTTGCCGGCACAGTT 74 GCG BPN68F AACTCTCACGGAACTCACNNSGCCGGCACAGTTGCG 75 GCT BPN69F TCTCACGGAACTCACGTTNNSGGCACAGTTGCGGCT 76 CTT BPN70F CACGGAACTCACGTTGCCNNSACAGTTGCGGCTCTT 77 AAT BPN71F GGAACTCACGTTGCCGGCNNSGTTGCGGCTCTTAAT 78 AAC BPN72F ACTCACGTTGCCGGCACANNSGCGGCTCTTAATAAC 79 TCA BPN73F CACGTTGCCGGCACAGTTNNSGCTCTTAATAACTCA 80 ATC BPN74F GTTGCCGGCACAGTTGCGNNSCTTAATAACTCAATC 81 GGT BPN75F GCCGGCACAGTTGCGGCTNNSAATAACTCAATCGGT 82 GTA BPN76F GGCACAGTTGCGGCTCTTNNSAACTCAATCGGTGTA 83 TTA BPN77F ACAGTTGCGGCTCTTAATNNSTCAATCGGTGTATTA 84 GGC BPN78F GTTGCGGCTCTTAATAACNNSATCGGTGTATTAGGC 85 GTT BPN79F GCGGCTCTTAATAACTCANNSGGTGTATTAGGCGTT 86 GCG BPN80F GCTCTTAATAACTCAATCNNSGTATTAGGCGTTGCG 87 CCA BPN81F CTTAATAACTCAATCGGTNNSTTAGGCGTTGCGCCA 88 AGC BPN82F AATAACTCAATCGGTGTANNSGGCGTTGCGCCAAGC 89 GCA BPN83F AACTCAATCGGTGTATTANNSGTTGCGCCAAGCGCA 90 TCA BPN84F TCAATCGGTGTATTAGGCNNSGCGCCAAGCGCATCA 91 CTT BPN85F ATCGGTGTATTAGGCGTTNNSCCAAGCGCATCACTT 92 TAC BPN86F GGTGTATTAGGCGTTGCGNNSAGCGCATCACTTTAC 93 GCT BPN87F GTATTAGGCGTTGCGCCANNSGCATCACTTTACGCT 94 GTA BPN88F TTAGGCGTTGCGCCAAGCNNSTCACTTTACGCTGTA 95 AAA BPN89F GGCGTTGCGCCAAGCGCANNSCTTTACGCTGTAAAA 96 GTT BPN90F GTTGCGCCAAGCGCATCANNSTACGCTGTAAAAGTT 97 CTC BPN91F GCGCCAAGCGCATCACTTNNSGCTGTAAAAGTTCTC 98 GGT BPN92F CCAAGCGCATCACTTTACNNSGTAAAAGTTCTCGGT 99 GCT BPN93F AGCGCATCACTTTACGCTNNSAAAGTTCTCGGTGCT 100 GAC BPN94F GCATCACTTTACGCTGTANNSGTTCTCGGTGCTGAC 101 GGT BPN95F TCACTTTACGCTGTAAAANNSCTCGGTGCTGACGGT 102 TCC BPN96F CTTTACGCTGTAAAAGTTNNSGGTGCTGACGGTTCC 103 GGC BPN97F TACGCTGTAAAAGTTCTCNNSGCTGACGGTTCCGGC 104 CAA BPN98F GCTGTAAAAGTTCTCGGTNNSGACGGTTCCGGCCAA 105 TAC BPN99F GTAAAAGTTCTCGGTGCTNNSGGTTCCGGCCAATAC 106 AGC BPN100F AAAGTTCTCGGTGCTGACNNSTCCGGCCAATACAGC 107 TGG BPN101F GTTCTCGGTGCTGACGGTNNSGGCCAATACAGCTGG 108 ATC BPN102F CTCGGTGCTGACGGTTCCNNSCAATACAGCTGGATC 109 ATT BPN103F GGTGCTGACGGTTCCGGCNNSTACAGCTGGATCATT 110 AAC BPN104F GCTGACGGTTCCGGCCAANNSAGCTGGATCATTAAC 111 GGA BPN105F GACGGTTCCGGCCAATACNNSTGGATCATTAACGGA 112 ATC BPN106F GGTTCCGGCCAATACAGCNNSATCATTAACGGAATC 113 GAG BPN107F TCCGGCCAATACAGCTGGNNSATTAACGGAATCGAG 114 TGG BPN108F GGCCAATACAGCTGGATCNNSAACGGAATCGAGTGG 115 GCG BPN109F CAATACAGCTGGATCATTNNSGGAATCGAGTGGGCG 116 ATC BPN110F TACAGCTGGATCATTAACNNSATCGAGTGGGCGATC 117 GCA BPN111F AGCTGGATCATTAACGGANNSGAGTGGGCGATCGCA 118 AAC BPN112F TGGATCATTAACGGAATCNNSTGGGCGATCGCAAAC 119 AAT BPN113F ATCATTAACGGAATCGAGNNSGCGATCGCAAACAAT 120 ATG BPN114F ATTAACGGAATCGAGTGGNNSATCGCAAACAATATG 121 GAC BPN115F AACGGAATCGAGTGGGCGNNSGCAAACAATATGGAC 122 GTT BPN116F GGAATCGAGTGGGCGATCNNSAACAATATGGACGTT 123 ATT BPN117F ATCGAGTGGGCGATCGCANNSAATATGGACGTTATT 124 AAC BPN118F GAGTGGGCGATCGCAAACNNSATGGACGTTATTAAC 125 ATG BPN119F TGGGCGATCGCAAACAATNNSGACGTTATTAACATG 126 AGC BPN120F GCGATCGCAAACAATATGNNSGTTATTAACATGAGC 127 CTC BPN121F ATCGCAAACAATATGGACNNSATTAACATGAGCCTC 128 GGC BPN122F GCAAACAATATGGACGTTNNSAACATGAGCCTCGGC 129 GGA BPN123F AACAATATGGACGTTATTNNSATGAGCCTCGGCGGA 130 CCT BPN124F AATATGGACGTTATTAACNNSAGCCTCGGCGGACCT 131 TCT BPN125F ATGGACGTTATTAACATGNNSCTCGGCGGACCTTCT 132 GGT BPN126F GACGTTATTAACATGAGCNNSGGCGGACCTTCTGGT 133 TCT BPN127F GTTATTAACATGAGCCTCNNSGGACCTTCTGGTTCT 134 GCT BPN128F ATTAACATGAGCCTCGGCNNSCCTTCTGGTTCTGCT 135 GCT BPN129F AACATGAGCCTCGGCGGANNSTCTGGTTCTGCTGCT 136 TTA BPN130F ATGAGCCTCGGCGGACCTNNSGGTTCTGCTGCTTTA 137 AAA BPN131F AGCCTCGGCGGACCTTCTNNSTCTGCTGCTTTAAAA 138 GCG BPN132F CTCGGCGGACCTTCTGGTNNSGCTGCTTTAAAAGCG 139 GCA BPN133F GGCGGACCTTCTGGTTCTNNSGCTTTAAAAGCGGCA 140 GTT BPN134F GGACCTTCTGGTTCTGCTNNSTTAAAAGCGGCAGTT 141 GAT BPN135F CCTTCTGGTTCTGCTGCTNNSAAAGCGGCAGTTGAT 142 AAA BPN136F TCTGGTTCTGCTGCTTTANNSGCGGCAGTTGATAAA 143 GCC BPN137F GGTTCTGCTGCTTTAAAANNSGCAGTTGATAAAGCC 144 GTT BPN138F TCTGCTGCTTTAAAAGCGNNSGTTGATAAAGCCGTT 145 GCA BPN139F GCTGCTTTAAAAGCGGCANNSGATAAAGCCGTTGCA 146 TCC BPN140F GCTTTAAAAGCGGCAGTTNNSAAAGCCGTTGCATCC 147 GGC BPN141F TTAAAAGCGGCAGTTGATNNSGCCGTTGCATCCGGC 148 GTC BPN142F AAAGCGGCAGTTGATAAANNSGTTGCATCCGGCGTC 149 GTA BPN143F GCGGCAGTTGATAAAGCCNNSGCATCCGGCGTCGTA 150 GTC BPN144F GCAGTTGATAAAGCCGTTNNSTCCGGCGTCGTAGTC 151 GTT BPN145F GTTGATAAAGCCGTTGCANNSGGCGTCGTAGTCGTT 152 GCG BPN146F GATAAAGCCGTTGCATCCNNSGTCGTAGTCGTTGCG 153 GCA BPN147F AAAGCCGTTGCATCCGGCNNSGTAGTCGTTGCGGCA 154 GCC BPN148F GCCGTTGCATCCGGCGTCNNSGTCGTTGCGGCAGCC 155 GGT BPN149F GTTGCATCCGGCGTCGTANNSGTTGCGGCAGCCGGT 156 AAC BPN150F GCATCCGGCGTCGTAGTCNNSGCGGCAGCCGGTAAC 157 GAA BPN151F TCCGGCGTCGTAGTCGTTNNSGCAGCCGGTAACGAA 158 GGC BPN152F GGCGTCGTAGTCGTTGCGNNSGCCGGTAACGAAGGC 159 ACT BPN153F GTCGTAGTCGTTGCGGCANNSGGTAACGAAGGCACT 160 TCC BPN154F GTAGTCGTTGCGGCAGCCNNSAACGAAGGCACTTCC 161 GGC BPN155F GTCGTTGCGGCAGCCGGTNNSGAAGGCACTTCCGGC 162 AGC BPN156F GTTGCGGCAGCCGGTAACNNSGGCACTTCCGGCAGC 163 TCA BPN157F GCGGCAGCCGGTAACGAANNSACTTCCGGCAGCTCA 164 AGC BPN158F GCAGCCGGTAACGAAGGCNNSTCCGGCAGCTCAAGC 165 ACA BPN159F GCCGGTAACGAAGGCACTNNSGGCAGCTCAAGCACA 166 GTG BPN160F GGTAACGAAGGCACTTCCNNSAGCTCAAGCACAGTG 167 GGC BPN161F AACGAAGGCACTTCCGGCNNSTCAAGCACAGTGGGC 168 TAC BPN162F GAAGGCACTTCCGGCAGCNNSAGCACAGTGGGCTAC 169 CCT BPN163F GGCACTTCCGGCAGCTCANNSACAGTGGGCTACCCT 170 GGT BPN164F ACTTCCGGCAGCTCAAGCNNSGTGGGCTACCCTGGT 171 AAA BPN165F TCCGGCAGCTCAAGCACANNSGGCTACCCTGGTAAA 172 TAC BPN166F GGCAGCTCAAGCACAGTGNNSTACCCTGGTAAATAC 173 CCT BPN167F AGCTCAAGCACAGTGGGCNNSCCTGGTAAATACCCT 174 TCT BPN168F TCAAGCACAGTGGGCTACNNSGGTAAATACCCTTCT 175 GTC BPN169F AGCACAGTGGGCTACCCTNNSAAATACCCTTCTGTC 176 ATT BPN170F ACAGTGGGCTACCCTGGTNNSTACCCTTCTGTCATT 177 GCA BPN171F GTGGGCTACCCTGGTAAANNSCCTTCTGTCATTGCA 178 GTA BPN172F GGCTACCCTGGTAAATACNNSTCTGTCATTGCAGTA 179 GGC BPN173F TACCCTGGTAAATACCCTNNSGTCATTGCAGTAGGC 180 GCT BPN174F CCTGGTAAATACCCTTCTNNSATTGCAGTAGGCGCT 181 GTT BPN175F GGTAAATACCCTTCTGTCNNSGCAGTAGGCGCTGTT 182 GAC BPN176F AAATACCCTTCTGTCATTNNSGTAGGCGCTGTTGAC 183 AGC BPN177F TACCCTTCTGTCATTGCANNSGGCGCTGTTGACAGC 184 AGC BPN178F CCTTCTGTCATTGCAGTANNSGCTGTTGACAGCAGC 185 AAC BPN179F TCTGTCATTGCAGTAGGCNNSGTTGACAGCAGCAAC 186 CAA BPN180F GTCATTGCAGTAGGCGCTNNSGACAGCAGCAACCAA 187 AGA BPN181F ATTGCAGTAGGCGCTGTTNNSAGCAGCAACCAAAGA 188 GCA BPN182F GCAGTAGGCGCTGTTGACNNSAGCAACCAAAGAGCA 189 TCT BPN183F GTAGGCGCTGTTGACAGCNNSAACCAAAGAGCATCT 190 TTC BPN184F GGCGCTGTTGACAGCAGCNNSCAAAGAGCATCTTTC 191 TCA BPN185F GCTGTTGACAGCAGCAACNNSAGAGCATCTTTCTCA 192 AGC BPN186F GTTGACAGCAGCAACCAANNSGCATCTTTCTCAAGC 193 GTA BPN187F GACAGCAGCAACCAAAGANNSTCTTTCTCAAGCGTA 194 GGA BPN188F AGCAGCAACCAAAGAGCANNSTTCTCAAGCGTAGGA 195 CCT BPN189F AGCAACCAAAGAGCATCTNNSTCAAGCGTAGGACCT 196 GAG BPN190F AACCAAAGAGCATCTTTCNNSAGCGTAGGACCTGAG 197 CTT BPN191F CAAAGAGCATCTTTCTCANNSGTAGGACCTGAGCTT 198 GAT BPN192F AGAGCATCTTTCTCAAGCNNSGGACCTGAGCTTGAT 199 GTC BPN193F GCATCTTTCTCAAGCGTANNSCCTGAGCTTGATGTC 200 ATG BPN194F TCTTTCTCAAGCGTAGGANNSGAGCTTGATGTCATG 201 GCA BPN195F TTCTCAAGCGTAGGACCTNNSCTTGATGTCATGGCA 202 CCT BPN196F TCAAGCGTAGGACCTGAGNNSGATGTCATGGCACCT 203 GGC BPN197F AGCGTAGGACCTGAGCTTNNSGTCATGGCACCTGGC 204 GTA BPN198F GTAGGACCTGAGCTTGATNNSATGGCACCTGGCGTA 205 TCT BPN199F GGACCTGAGCTTGATGTCNNSGCACCTGGCGTATCT 206 ATC BPN200F CCTGAGCTTGATGTCATGNNSCCTGGCGTATCTATC 207 CAA BPN201F GAGCTTGATGTCATGGCANNSGGCGTATCTATCCAA 208 AGC BPN202F CTTGATGTCATGGCACCTNNSGTATCTATCCAAAGC 209 ACG BPN203F GATGTCATGGCACCTGGCNNSTCTATCCAAAGCACG 210 CTT BPN204F GTCATGGCACCTGGCGTANNSATCCAAAGCACGCTT 211 CCT BPN205F ATGGCACCTGGCGTATCTNNSCAAAGCACGCTTCCT 212 GGA BPN206F GCACCTGGCGTATCTATCNNSAGCACGCTTCCTGGA 213 AAC BPN207F CCTGGCGTATCTATCCAANNSACGCTTCCTGGAAAC 214 AAA BPN208F GGCGTATCTATCCAAAGCNNSCTTCCTGGAAACAAA 215 TAC BPN209F GTATCTATCCAAAGCACGNNSCCTGGAAACAAATAC 216 GGG BPN210F TCTATCCAAAGCACGCTTNNSGGAAACAAATACGGG 217 GCG BPN211F ATCCAAAGCACGCTTCCTNNSAACAAATACGGGGCG 218 TAC BPN212F CAAAGCACGCTTCCTGGANNSAAATACGGGGCGTAC 219 AAC BPN213F AGCACGCTTCCTGGAAACNNSTACGGGGCGTACAAC 220 GGT BPN214F ACGCTTCCTGGAAACAAANNSGGGGCGTACAACGGT 221 ACG BPN215F CTTCCTGGAAACAAATACNNSGCGTACAACGGTACG 222 TCA BPN216F CCTGGAAACAAATACGGGNNSTACAACGGTACGTCA 223 ATG BPN217F GGAAACAAATACGGGGCGNNSAACGGTACGTCAATG 224 GCA BPN218F AACAAATACGGGGCGTACNNSGGTACGTCAATGGCA 225 TCT BPN219F AAATACGGGGCGTACAACNNSACGTCAATGGCATCT 226 CCG BPN220F TACGGGGCGTACAACGGTNNSTCAATGGCATCTCCG 227 CAC BPN221F GGGGCGTACAACGGTACGNNSATGGCATCTCCGCAC 228 GTT BPN222F GCGTACAACGGTACGTCANNSGCATCTCCGCACGTT 229 GCC BPN223F TACAACGGTACGTCAATGNNSTCTCCGCACGTTGCC 230 GGA BPN224F AACGGTACGTCAATGGCANNSCCGCACGTTGCCGGA 231 GCG BPN225F GGTACGTCAATGGCATCTNNSCACGTTGCCGGAGCG 232 GCT BPN226F ACGTCAATGGCATCTCCGNNSGTTGCCGGAGCGGCT 233 GCT BPN227F TCAATGGCATCTCCGCACNNSGCCGGAGCGGCTGCT 234 TTG BPN228F ATGGCATCTCCGCACGTTNNSGGAGCGGCTGCTTTG 235 ATT BPN229F GCATCTCCGCACGTTGCCNNSGCGGCTGCTTTGATT 236 CTT BPN230F TCTCCGCACGTTGCCGGANNSGCTGCTTTGATTCTT 237 TCT BPN231F CCGCACGTTGCCGGAGCGNNSGCTTTGATTCTTTCT 238 AAG BPN232F CACGTTGCCGGAGCGGCTNNSTTGATTCTTTCTAAG 239 CAC BPN233F GTTGCCGGAGCGGCTGCTNNSATTCTTTCTAAGCAC 240 CCG BPN234F GCCGGAGCGGCTGCTTTGNNSCTTTCTAAGCACCCG 241 AAC BPN235F GGAGCGGCTGCTTTGATTNNSTCTAAGCACCCGAAC 242 TGG BPN236F GCGGCTGCTTTGATTCTTNNSAAGCACCCGAACTGG 243 ACA BPN237F GCTGCTTTGATTCTTTCTNNSCACCCGAACTGGACA 244 AAC BPN238F GCTTTGATTCTTTCTAAGNNSCCGAACTGGACAAAC 245 ACT BPN239F TTGATTCTTTCTAAGCACNNSAACTGGACAAACACT 246 CAA BPN240F ATTCTTTCTAAGCACCCGNNSTGGACAAACACTCAA 247 GTC BPN241F CTTTCTAAGCACCCGAACNNSACAAACACTCAAGTC 248 CGC BPN242F TCTAAGCACCCGAACTGGNNSAACACTCAAGTCCGC 249 AGC BPN243F AAGCACCCGAACTGGACANNSACTCAAGTCCGCAGC 250 AGT BPN244F CACCCGAACTGGACAAACNNSCAAGTCCGCAGCAGT 251 TTA BPN245F CCGAACTGGACAAACACTNNSGTCCGCAGCAGTTTA 252 GAA BPN246F AACTGGACAAACACTCAANNSCGCAGCAGTTTAGAA 253 AAC BPN247F TGGACAAACACTCAAGTCNNSAGCAGTTTAGAAAAC 254 ACC BPN248F ACAAACACTCAAGTCCGCNNSAGTTTAGAAAACACC 255 ACT BPN249F AACACTCAAGTCCGCAGCNNSTTAGAAAACACCACT 256 ACA BPN250F ACTCAAGTCCGCAGCAGTNNSGAAAACACCACTACA 257 AAA BPN251F CAAGTCCGCAGCAGTTTANNSAACACCACTACAAAA 258 CTT BPN252F GTCCGCAGCAGTTTAGAANNSACCACTACAAAACTT 259 GGT BPN253F CGCAGCAGTTTAGAAAACNNSACTACAAAACTTGGT 260 GAT BPN254F AGCAGTTTAGAAAACACCNNSACAAAACTTGGTGAT 261 TCT BPN255F AGTTTAGAAAACACCACTNNSAAACTTGGTGATTCT 262 TTC BPN256F TTAGAAAACACCACTACANNSCTTGGTGATTCTTTC 263 TAC BPN257F GAAAACACCACTACAAAANNSGGTGATTCTTTCTAC 264 TAT BPN258F AACACCACTACAAAACTTNNSGATTCTTTCTACTAT 265 GGA BPN259F ACCACTACAAAACTTGGTNNSTCTTTCTACTATGGA 266 AAA BPN260F ACTACAAAACTTGGTGATNNSTTCTACTATGGAAAA 267 GGG BPN261F ACAAAACTTGGTGATTCTNNSTACTATGGAAAAGGG 268 CTG BPN262F AAACTTGGTGATTCTTTCNNSTATGGAAAAGGGCTG 269 ATC BPN263F CTTGGTGATTCTTTCTACNNSGGAAAAGGGCTGATC 270 AAC BPN264F GGTGATTCTTTCTACTATNNSAAAGGGCTGATCAAC 271 GTA BPN265F GATTCTTTCTACTATGGANNSGGGCTGATCAACGTA 272 CAG BPN266F TCTTTCTACTATGGAAAANNSCTGATCAACGTACAG 273 GCG BPN267F TTCTACTATGGAAAAGGGNNSATCAACGTACAGGCG 274 GCA BPN268F TACTATGGAAAAGGGCTGNNSAACGTACAGGCGGCA 275 GCT BPN269F TATGGAAAAGGGCTGATCNNSGTACAGGCGGCAGCT 276 CAG BPN270F GGAAAAGGGCTGATCAACNNSCAGGCGGCAGCTCAG 277 TAA BPN271F AAAGGGCTGATCAACGTANNSGCGGCAGCTCAGTAA 278 AGC BPN272F GGGCTGATCAACGTACAGNNSGCAGCTCAGTAAAGC 279 TTA BPN273F CTGATCAACGTACAGGCGNNSGCTCAGTAAAGCTTA 280 CTG BPN274F ATCAACGTACAGGCGGCANNSCAGTAAAGCTTACTG 281 GCC BPN275F AACGTACAGGCGGCAGCTNNSTAAAGCTTACTGGCC 282 GTC BPN1R GCCGTAAGGCACGGACTGSNNGTATGCATGTGCTAC 283 GTG BPN2R TACGCCGTAAGGCACGGASNNCGCGTATGCATGTGC 284 TAC BPN3R TGATACGCCGTAAGGCACSNNCTGCGCGTATGCATG 285 TGC BPN4R TTGTGATACGCCGTAAGGSNNGGACTGCGCGTATGC 286 ATG BPN5R AATTTGTGATACGCCGTASNNCACGGACTGCGCGTA 287 TGC BPN6R TTTAATTTGTGATACGCCSNNAGGCACGGACTGCGC 288 GTA BPN7R GGCTTTAATTTGTGATACSNNGTAAGGCACGGACTG 289 CGC BPN8R AGGGGCTTTAATTTGTGASNNGCCGTAAGGCACGGA 290 CTG BPN9R AGCAGGGGCTTTAATTTGSNNTACGCCGTAAGGCAC 291 GGA BPN10R CAGAGCAGGGGCTTTAATSNNTGATACGCCGTAAGG 292 CAC BPN11R GTGCAGAGCAGGGGCTTTSNNTTGTGATACGCCGTA 293 AGG BPN12R AGAGTGCAGAGCAGGGGCSNNAATTTGTGATACGCC 294 GTA BPN13R TTGAGAGTGCAGAGCAGGSNNTTTAATTTGTGATAC 295 GCC BPN14R GCCTTGAGAGTGCAGAGCSNNGGCTTTAATTTGTGA 296 TAC BPN15R GTAGCCTTGAGAGTGCAGSNNAGGGGCTTTAATTTG 297 TGA BPN16R AGTGTAGCCTTGAGAGTGSNNAGCAGGGGCTTTAAT 298 TTG BPN17R TCCAGTGTAGCCTTGAGASNNCAGAGCAGGGGCTTT 299 AAT BPN18R TGATCCAGTGTAGCCTTGSNNGTGCAGAGCAGGGGC 300 TTT BPN19R ATTTGATCCAGTGTAGCCSNNAGAGTGCAGAGCAGG 301 GGC BPN20R AACATTTGATCCAGTGTASNNTTGAGAGTGCAGAGC 302 AGG BPN21R TTTAACATTTGATCCAGTSNNGCCTTGAGAGTGCAG 303 AGC BPN22R TACTTTAACATTTGATCCSNNGTAGCCTTGAGAGTG 304 CAG BPN23R CGCTACTTTAACATTTGASNNAGTGTAGCCTTGAGA 305 GTG BPN24R AACCGCTACTTTAACATTSNNTCCAGTGTAGCCTTG 306 AGA BPN25R GATAACCGCTACTTTAACSNNTGATCCAGTGTAGCC 307 TTG BPN26R GTCGATAACCGCTACTTTSNNATTTGATCCAGTGTA 308 GCC BPN27R GCTGTCGATAACCGCTACSNNAACATTTGATCCAGT 309 GTA BPN28R ACCGCTGTCGATAACCGCSNNTTTAACATTTGATCC 310 AGT BPN29R GATACCGCTGTCGATAACSNNTACTTTAACATTTGA 311 TCC BPN30R ATCGATACCGCTGTCGATSNNCGCTACTTTAACATT 312 TGA BPN31R AGAATCGATACCGCTGTCSNNAACCGCTACTTTAAC 313 ATT BPN32R AGAAGAATCGATACCGCTSNNGATAACCGCTACTTT 314 AAC BPN33R ATGAGAAGAATCGATACCSNNGTCGATAACCGCTAC 315 TTT BPN34R AGGATGAGAAGAATCGATSNNGCTGTCGATAACCGC 316 TAC BPN35R ATCAGGATGAGAAGAATCSNNACCGCTGTCGATAAC 317 CGC BPN36R TAAATCAGGATGAGAAGASNNGATACCGCTGTCGAT 318 AAC BPN37R CTTTAAATCAGGATGAGASNNATCGATACCGCTGTC 319 GAT BPN38R TACCTTTAAATCAGGATGSNNAGAATCGATACCGCT 320 GTC BPN39R TGCTACCTTTAAATCAGGSNNAGAAGAATCGATACC 321 GCT BPN40R GCCTGCTACCTTTAAATCSNNATGAGAAGAATCGAT 322 ACC BPN41R TCCGCCTGCTACCTTTAASNNAGGATGAGAAGAATC 323 GAT BPN42R GGCTCCGCCTGCTACCTTSNNATCAGGATGAGAAGA 324 ATC BPN43R GCTGGCTCCGCCTGCTACSNNTAAATCAGGATGAGA 325 AGA BPN44R CATGCTGGCTCCGCCTGCSNNCTTTAAATCAGGATG 326 AGA BPN45R AACCATGCTGGCTCCGCCSNNTACCTTTAAATCAGG 327 ATG BPN46R AGGAACCATGCTGGCTCCSNNTGCTACCTTTAAATC 328 AGG BPN47R AGAAGGAACCATGCTGGCSNNGCCTGCTACCTTTAA 339 ATC BPN48R TTCAGAAGGAACCATGCTSNNTCCGCCTGCTACCTT 330 TAA BPN49R TGTTTCAGAAGGAACCATSNNGGCTCCGCCTGCTAC 331 CTT BPN50R ATTTGTTTCAGAAGGAACSNNGCTGGCTCCGCCTGC 332 TAC BPN51R AGGATTTGTTTCAGAAGGSNNCATGCTGGCTCCGCC 333 TGC BPN52R GAAAGGATTTGTTTCAGASNNAACCATGCTGGCTCC 334 GCC BPN53R TTGGAAAGGATTTGTTTCSNNAGGAACCATGCTGGC 335 TCC BPN54R GTCTTGGAAAGGATTTGTSNNAGAAGGAACCATGCT 336 GGC BPN55R GTTGTCTTGGAAAGGATTSNNTTCAGAAGGAACCAT 337 GCT BPN56R GTTGTTGTCTTGGAAAGGSNNTGTTTCAGAAGGAAC 338 CAT BPN57R AGAGTTGTTGTCTTGGAASNNATTTGTTTCAGAAGG 339 AAC BPN58R GTGAGAGTTGTTGTCTTGSNNAGGATTTGTTTCAGA 340 AGG BPN59R TCCGTGAGAGTTGTTGTCSNNGAAAGGATTTGTTTC 341 AGA BPN60R AGTTCCGTGAGAGTTGTTSNNTTGGAAAGGATTTGT 342 TTC BPN61R GTGAGTTCCGTGAGAGTTSNNGTCTTGGAAAGGATT 343 TGT BPN62R AACGTGAGTTCCGTGAGASNNGTTGTCTTGGAAAGG 344 ATT BPN63R GGCAACGTGAGTTCCGTGSNNGTTGTTGTCTTGGAA 345 AGG BPN64R GCCGGCAACGTGAGTTCCSNNAGAGTTGTTGTCTTG 346 GAA BPN65R TGTGCCGGCAACGTGAGTSNNGTGAGAGTTGTTGTC 347 TTG BPN66R AACTGTGCCGGCAACGTGSNNTCCGTGAGAGTTGTT 348 GTC BPN67R CGCAACTGTGCCGGCAACSNNAGTTCCGTGAGAGTT 349 GTT BPN68R AGCCGCAACTGTGCCGGCSNNGTGAGTTCCGTGAGA 350 GTT BPN69R AAGAGCCGCAACTGTGCCSNNAACGTGAGTTCCGTG 351 AGA BPN70R ATTAAGAGCCGCAACTGTSNNGGCAACGTGAGTTCC 352 GTG BPN71R GTTATTAAGAGCCGCAACSNNGCCGGCAACGTGAGT 353 TCC BPN72R TGAGTTATTAAGAGCCGCSNNTGTGCCGGCAACGTG 354 AGT BPN73R GATTGAGTTATTAAGAGCSNNAACTGTGCCGGCAAC 355 GTG BPN74R ACCGATTGAGTTATTAAGSNNCGCAACTGTGCCGGC 356 AAC BPN75R TACACCGATTGAGTTATTSNNAGCCGCAACTGTGCC 357 GGC BPN76R TAATACACCGATTGAGTTSNNAAGAGCCGCAACTGT 358 GCC BPN77R GCCTAATACACCGATTGASNNATTAAGAGCCGCAAC 359 TGT BPN78R AACGCCTAATACACCGATSNNGTTATTAAGAGCCGC 360 AAC BPN79R CGCAACGCCTAATACACCSNNTGAGTTATTAAGAGC 361 CGC BPN80R TGGCGCAACGCCTAATACSNNGATTGAGTTATTAAG 362 AGC BPN81R GCTTGGCGCAACGCCTAASNNACCGATTGAGTTATT 363 AAG BPN82R TGCGCTTGGCGCAACGCCSNNTACACCGATTGAGTT 364 ATT BPN83R TGATGCGCTTGGCGCAACSNNTAATACACCGATTGA 365 GTT BPN84R AAGTGATGCGCTTGGCGCSNNGCCTAATACACCGAT 366 TGA BPN85R GTAAAGTGATGCGCTTGGSNNAACGCCTAATACACC 367 GAT BPN86R AGCGTAAAGTGATGCGCTSNNCGCAACGCCTAATAC 368 ACC BPN87R TACAGCGTAAAGTGATGCSNNTGGCGCAACGCCTAA 369 TAC BPN88R TTTTACAGCGTAAAGTGASNNGCTTGGCGCAACGCC 370 TAA BPN89R AACTTTTACAGCGTAAAGSNNTGCGCTTGGCGCAAC 371 GCC BPN90R GAGAACTTTTACAGCGTASNNTGATGCGCTTGGCGC 372 AAC BPN91R ACCGAGAACTTTTACAGCSNNAAGTGATGCGCTTGG 373 CGC BPN92R AGCACCGAGAACTTTTACSNNGTAAAGTGATGCGCT 374 TGG BPN93R GTCAGCACCGAGAACTTTSNNAGCGTAAAGTGATGC 375 GCT BPN94R ACCGTCAGCACCGAGAACSNNTACAGCGTAAAGTGA 376 TGC BPN95R GGAACCGTCAGCACCGAGSNNTTTTACAGCGTAAAG 377 TGA BPN96R GCCGGAACCGTCAGCACCSNNAACTTTTACAGCGTA 378 AAG BPN97R TTGGCCGGAACCGTCAGCSNNGAGAACTTTTACAGC 379 GTA BPN98R GTATTGGCCGGAACCGTCSNNACCGAGAACTTTTAC 380 AGC BPN99R GCTGTATTGGCCGGAACCSNNAGCACCGAGAACTTT 381 TAC BPN100R CCAGCTGTATTGGCCGGASNNGTCAGCACCGAGAAC 382 TTT BPN101R GATCCAGCTGTATTGGCCSNNACCGTCAGCACCGAG 383 AAC BPN102R AATGATCCAGCTGTATTGSNNGGAACCGTCAGCACC 384 GAG BPN103R GTTAATGATCCAGCTGTASNNGCCGGAACCGTCAGC 385 ACC BPN104R TCCGTTAATGATCCAGCTSNNTTGGCCGGAACCGTC 386 AGC BPN105R GATTCCGTTAATGATCCASNNGTATTGGCCGGAACC 387 GTC BPN106R CTCGATTCCGTTAATGATSNNGCTGTATTGGCCGGA 388 ACC BPN107R CCACTCGATTCCGTTAATSNNCCAGCTGTATTGGCC 389 GGA BPN108R CGCCCACTCGATTCCGTTSNNGATCCAGCTGTATTG 390 GCC BPN109R GATCGCCCACTCGATTCCSNNAATGATCCAGCTGTA 391 TTG BPN110R TGCGATCGCCCACTCGATSNNGTTAATGATCCAGCT 392 GTA BPN111R GTTTGCGATCGCCCACTCSNNTCCGTTAATGATCCA 393 GCT BPN112R ATTGTTTGCGATCGCCCASNNGATTCCGTTAATGAT 394 CCA BPN113R CATATTGTTTGCGATCGCSNNCTCGATTCCGTTAAT 395 GAT BPN114R GTCCATATTGTTTGCGATSNNCCACTCGATTCCGTT 396 AAT BPN115R AACGTCCATATTGTTTGCSNNCGCCCACTCGATTCC 397 GTT BPN116R AATAACGTCCATATTGTTSNNGATCGCCCACTCGAT 398 TCC BPN117R GTTAATAACGTCCATATTSNNTGCGATCGCCCACTC 399 GAT BPN118R CATGTTAATAACGTCCATSNNGTTTGCGATCGCCCA 401 CTC BPN119R GCTCATGTTAATAACGTCSNNATTGTTTGCGATCGC 402 CCA BPN120R GAGGCTCATGTTAATAACSNNCATATTGTTTGCGAT 403 CGC BPN121R GCCGAGGCTCATGTTAATSNNGTCCATATTGTTTGC 404 GAT BPN122R TCCGCCGAGGCTCATGTTSNNAACGTCCATATTGTT 405 TGC BPN123R AGGTCCGCCGAGGCTCATSNNAATAACGTCCATATT 406 GTT BPN124R AGAAGGTCCGCCGAGGCTSNNGTTAATAACGTCCAT 407 ATT BPN125R ACCAGAAGGTCCGCCGAGSNNCATGTTAATAACGTC 408 CAT BPN126R AGAACCAGAAGGTCCGCCSNNGCTCATGTTAATAAC 409 GTC BPN127R AGCAGAACCAGAAGGTCCSNNGAGGCTCATGTTAAT 410 AAC BPN128R AGCAGCAGAACCAGAAGGSNNGCCGAGGCTCATGTT 411 AAT BPN129R TAAAGCAGCAGAACCAGASNNTCCGCCGAGGCTCAT 412 GTT BPN130R TTTTAAAGCAGCAGAACCSNNAGGTCCGCCGAGGCT 413 CAT BPN131R CGCTTTTAAAGCAGCAGASNNAGAAGGTCCGCCGAG 414 GCT BPN132R TGCCGCTTTTAAAGCAGCSNNACCAGAAGGTCCGCC 415 GAG BPN133R AACTGCCGCTTTTAAAGCSNNAGAACCAGAAGGTCC 416 GCC BPN134R ATCAACTGCCGCTTTTAASNNAGCAGAACCAGAAGG 417 TCC BPN135R TTTATCAACTGCCGCTTTSNNAGCAGCAGAACCAGA 418 AGG BPN136R GGCTTTATCAACTGCCGCSNNTAAAGCAGCAGAACC 419 AGA BPN137R AACGGCTTTATCAACTGCSNNTTTTAAAGCAGCAGA 420 ACC BPN138R TGCAACGGCTTTATCAACSNNCGCTTTTAAAGCAGC 421 AGA BPN139R GGATGCAACGGCTTTATCSNNTGCCGCTTTTAAAGC 422 AGC BPN140R GCCGGATGCAACGGCTTTSNNAACTGCCGCTTTTAA 423 AGC BPN141R GACGCCGGATGCAACGGCSNNATCAACTGCCGCTTT 424 TAA BPN142R TACGACGCCGGATGCAACSNNTTTATCAACTGCCGC 425 TTT BPN143R GACTACGACGCCGGATGCSNNGGCTTTATCAACTGC 426 CGC BPN144R AACGACTACGACGCCGGASNNAACGGCTTTATCAAC 427 TGC BPN145R CGCAACGACTACGACGCCSNNTGCAACGGCTTTATC 428 AAC BPN146R TGCCGCAACGACTACGACSNNGGATGCAACGGCTTT 429 ATC BPN147R GGCTGCCGCAACGACTACSNNGCCGGATGCAACGGC 430 TTT BPN148R ACCGGCTGCCGCAACGACSNNGACGCCGGATGCAAC 431 GGC BPN149R GTTACCGGCTGCCGCAACSNNTACGACGCCGGATGC 432 AAC BPN150R TTCGTTACCGGCTGCCGCSNNGACTACGACGCCGGA 433 TGC BPN151R GCCTTCGTTACCGGCTGCSNNAACGACTACGACGCC 434 GGA BPN152R AGTGCCTTCGTTACCGGCSNNCGCAACGACTACGAC 435 GCC BPN153R GGAAGTGCCTTCGTTACCSNNTGCCGCAACGACTAC 436 GAC BPN154R GCCGGAAGTGCCTTCGTTSNNGGCTGCCGCAACGAC 437 TAC BPN155R GCTGCCGGAAGTGCCTTCSNNACCGGCTGCCGCAAC 438 GAC BPN156R TGAGCTGCCGGAAGTGCCSNNGTTACCGGCTGCCGC 439 AAC BPN157R GCTTGAGCTGCCGGAAGTSNNTTCGTTACCGGCTGC 440 CGC BPN158R TGTGCTTGAGCTGCCGGASNNGCCTTCGTTACCGGC 441 TGC BPN159R CACTGTGCTTGAGCTGCCSNNAGTGCCTTCGTTACC 442 GGC BPN160R GCCCACTGTGCTTGAGCTSNNGGAAGTGCCTTCGTT 443 ACC BPN161R GTAGCCCACTGTGCTTGASNNGCCGGAAGTGCCTTC 444 GTT BPN162R AGGGTAGCCCACTGTGCTSNNGCTGCCGGAAGTGCC 445 TTC BPN163R ACCAGGGTAGCCCACTGTSNNTGAGCTGCCGGAAGT 446 GCC BPN164R TTTACCAGGGTAGCCCACSNNGCTTGAGCTGCCGGA 447 AGT BPN165R GTATTTACCAGGGTAGCCSNNTGTGCTTGAGCTGCC 448 GGA BPN166R AGGGTATTTACCAGGGTASNNCACTGTGCTTGAGCT 449 GCC BPN167R AGAAGGGTATTTACCAGGSNNGCCCACTGTGCTTGA 450 GCT BPN168R GACAGAAGGGTATTTACCSNNGTAGCCCACTGTGCT 451 TGA BPN169R AATGACAGAAGGGTATTTSNNAGGGTAGCCCACTGT 452 GCT BPN170R TGCAATGACAGAAGGGTASNNACCAGGGTAGCCCAC 453 TGT BPN171R TACTGCAATGACAGAAGGSNNTTTACCAGGGTAGCC 454 CAC BPN172R GCCTACTGCAATGACAGASNNGTATTTACCAGGGTA 455 GCC BPN173R AGCGCCTACTGCAATGACSNNAGGGTATTTACCAGG 456 GTA BPN174R AACAGCGCCTACTGCAATSNNAGAAGGGTATTTACC 457 AGG BPN175R GTCAACAGCGCCTACTGCSNNGACAGAAGGGTATTT 458 ACC BPN176R GCTGTCAACAGCGCCTACSNNAATGACAGAAGGGTA 459 TTT BPN177R GCTGCTGTCAACAGCGCCSNNTGCAATGACAGAAGG 460 GTA BPN178R GTTGCTGCTGTCAACAGCSNNTACTGCAATGACAGA 461 AGG BPN179R TTGGTTGCTGCTGTCAACSNNGCCTACTGCAATGAC 462 AGA BPN180R TCTTTGGTTGCTGCTGTCSNNAGCGCCTACTGCAAT 463 GAC BPN181R TGCTCTTTGGTTGCTGCTSNNAACAGCGCCTACTGC 464 AAT BPN182R AGATGCTCTTTGGTTGCTSNNGTCAACAGCGCCTAC 465 TGC BPN183R GAAAGATGCTCTTTGGTTSNNGCTGTCAACAGCGCC 466 TAC BPN184R TGAGAAAGATGCTCTTTGSNNGCTGCTGTCAACAGC 467 GCC BPN185R GCTTGAGAAAGATGCTCTSNNGTTGCTGCTGTCAAC 468 AGC BPN186R TACGCTTGAGAAAGATGCSNNTTGGTTGCTGCTGTC 469 AAC BPN187R TCCTACGCTTGAGAAAGASNNTCTTTGGTTGCTGCT 470 GTC BPN188R AGGTCCTACGCTTGAGAASNNTGCTCTTTGGTTGCT 471 GCT BPN189R CTCAGGTCCTACGCTTGASNNAGATGCTCTTTGGTT 472 GCT BPN190R AAGCTCAGGTCCTACGCTSNNGAAAGATGCTCTTTG 473 GTT BPN191R ATCAAGCTCAGGTCCTACSNNTGAGAAAGATGCTCT 474 TTG BPN192R GACATCAAGCTCAGGTCCSNNGCTTGAGAAAGATGC 475 TCT BPN193R CATGACATCAAGCTCAGGSNNTACGCTTGAGAAAGA 476 TGC BPN194R TGCCATGACATCAAGCTCSNNTCCTACGCTTGAGAA 477 AGA BPN195R AGGTGCCATGACATCAAGSNNAGGTCCTACGCTTGA 478 GAA BPN196R GCCAGGTGCCATGACATCSNNCTCAGGTCCTACGCT 479 TGA BPN197R TACGCCAGGTGCCATGACSNNAAGCTCAGGTCCTAC 480 GCT BPN198R AGATACGCCAGGTGCCATSNNATCAAGCTCAGGTCC 481 TAC BPN199R GATAGATACGCCAGGTGCSNNGACATCAAGCTCAGG 482 TCC BPN200R TTGGATAGATACGCCAGGSNNCATGACATCAAGCTC 483 AGG BPN201R GCTTTGGATAGATACGCCSNNTGCCATGACATCAAG 484 CTC BPN202R CGTGCTTTGGATAGATACSNNAGGTGCCATGACATC 485 AAG BPN203R AAGCGTGCTTTGGATAGASNNGCCAGGTGCCATGAC 486 ATC BPN204R AGGAAGCGTGCTTTGGATSNNTACGCCAGGTGCCAT 487 GAC BPN205R TCCAGGAAGCGTGCTTTGSNNAGATACGCCAGGTGC 488 CAT BPN206R GTTTCCAGGAAGCGTGCTSNNGATAGATACGCCAGG 489 TGC BPN207R TTTGTTTCCAGGAAGCGTSNNTTGGATAGATACGCC 490 AGG BPN208R GTATTTGTTTCCAGGAAGSNNGCTTTGGATAGATAC 491 GCC BPN209R CCCGTATTTGTTTCCAGGSNNCGTGCTTTGGATAGA 492 TAC BPN210R CGCCCCGTATTTGTTTCCSNNAAGCGTGCTTTGGAT 493 AGA BPN211R GTACGCCCCGTATTTGTTSNNAGGAAGCGTGCTTTG 494 GAT BPN212R GTTGTACGCCCCGTATTTSNNTCCAGGAAGCGTGCT 495 TTG BPN213R ACCGTTGTACGCCCCGTASNNGTTTCCAGGAAGCGT 496 GCT BPN214R CGTACCGTTGTACGCCCCSNNTTTGTTTCCAGGAAG 497 CGT BPN215R TGACGTACCGTTGTACGCSNNGTATTTGTTTCCAGG 498 AAG BPN216R CATTGACGTACCGTTGTASNNCCCGTATTTGTTTCC 499 AGG BPN217R TGCCATTGACGTACCGTTSNNCGCCCCGTATTTGTT 500 TCC BPN218R AGATGCCATTGACGTACCSNNGTACGCCCCGTATTT 501 GTT BPN219R CGGAGATGCCATTGACGTSNNGTTGTACGCCCCGTA 502 TTT BPN220R GTGCGGAGATGCCATTGASNNACCGTTGTACGCCCC 503 GTA BPN221R AACGTGCGGAGATGCCATSNNCGTACCGTTGTACGC 504 CCC BPN222R GGCAACGTGCGGAGATGCSNNTGACGTACCGTTGTA 505 CGC BPN223R TCCGGCAACGTGCGGAGASNNCATTGACGTACCGTT 506 GTA BPN224R CGCTCCGGCAACGTGCGGSNNTGCCATTGACGTACC 507 GTT BPN225R AGCCGCTCCGGCAACGTGSNNAGATGCCATTGACGT 508 ACC BPN226R AGCAGCCGCTCCGGCAACSNNCGGAGATGCCATTGA 509 CGT BPN227R CAAAGCAGCCGCTCCGGCSNNGTGCGGAGATGCCAT 510 TGA BPN228R AATCAAAGCAGCCGCTCCSNNAACGTGCGGAGATGC 511 CAT BPN229R AAGAATCAAAGCAGCCGCSNNGGCAACGTGCGGAGA 512 TGC BPN230R AGAAAGAATCAAAGCAGCSNNTCCGGCAACGTGCGG 513 AGA BPN231R CTTAGAAAGAATCAAAGCSNNCGCTCCGGCAACGTG 514 CGG BPN232R GTGCTTAGAAAGAATCAASNNAGCCGCTCCGGCAAC 515 GTG BPN233R CGGGTGCTTAGAAAGAATSNNAGCAGCCGCTCCGGC 516 AAC BPN234R GTTCGGGTGCTTAGAAAGSNNCAAAGCAGCCGCTCC 517 GGC BPN235R CCAGTTCGGGTGCTTAGASNNAATCAAAGCAGCCGC 518 TCC BPN236R TGTCCAGTTCGGGTGCTTSNNAAGAATCAAAGCAGC 519 CGC BPN237R GTTTGTCCAGTTCGGGTGSNNAGAAAGAATCAAAGC 520 AGC BPN238R AGTGTTTGTCCAGTTCGGSNNCTTAGAAAGAATCAA 521 AGC BPN239R TTGAGTGTTTGTCCAGTTSNNGTGCTTAGAAAGAAT 522 CAA BPN240R GACTTGAGTGTTTGTCCASNNCGGGTGCTTAGAAAG 523 AAT BPN241R GCGGACTTGAGTGTTTGTSNNGTTCGGGTGCTTAGA 524 AAG BPN242R GCTGCGGACTTGAGTGTTSNNCCAGTTCGGGTGCTT 525 AGA BPN243R ACTGCTGCGGACTTGAGTSNNTGTCCAGTTCGGGTG 526 CTT BPN244R TAAACTGCTGCGGACTTGSNNGTTTGTCCAGTTCGG 527 GTG BPN245R TTCTAAACTGCTGCGGACSNNAGTGTTTGTCCAGTT 528 CGG BPN246R GTTTTCTAAACTGCTGCGSNNTTGAGTGTTTGTCCA 529 GTT BPN247R GGTGTTTTCTAAACTGCTSNNGACTTGAGTGTTTGT 530 CCA BPN248R AGTGGTGTTTTCTAAACTSNNGCGGACTTGAGTGTT 531 TGT BPN249R TGTAGTGGTGTTTTCTAASNNGCTGCGGACTTGAGT 532 GTT BPN250R TTTTGTAGTGGTGTTTTCSNNACTGCTGCGGACTTG 533 AGT BPN251R AAGTTTTGTAGTGGTGTTSNNTAAACTGCTGCGGAC 534 TTG BPN252R ACCAAGTTTTGTAGTGGTSNNTTCTAAACTGCTGCG 535 GAC BPN253R ATCACCAAGTTTTGTAGTSNNGTTTTCTAAACTGCT 536 GCG BPN254R AGAATCACCAAGTTTTGTSNNGGTGTTTTCTAAACT 537 GCT BPN255R GAAAGAATCACCAAGTTTSNNAGTGGTGTTTTCTAA 538 ACT BPN256R GTAGAAAGAATCACCAAGSNNTGTAGTGGTGTTTTC 539 TAA BPN257R ATAGTAGAAAGAATCACCSNNTTTTGTAGTGGTGTT 540 TTC BPN258R TCCATAGTAGAAAGAATCSNNAAGTTTTGTAGTGGT 541 GTT BPN259R TTTTCCATAGTAGAAAGASNNACCAAGTTTTGTAGT 542 GGT BPN260R CCCTTTTCCATAGTAGAASNNATCACCAAGTTTTGT 543 AGT BPN261R CAGCCCTTTTCCATAGTASNNAGAATCACCAAGTTT 544 TGT BPN262R GATCAGCCCTTTTCCATASNNGAAAGAATCACCAAG 545 TTT BPN263R GTTGATCAGCCCTTTTCCSNNGTAGAAAGAATCACC 546 AAG BPN264R TACGTTGATCAGCCCTTTSNNATAGTAGAAAGAATC 547 ACC BPN265R CTGTACGTTGATCAGCCCSNNTCCATAGTAGAAAGA 548 ATC BPN266R CGCCTGTACGTTGATCAGSNNTTTTCCATAGTAGAA 549 AGA BPN267R TGCCGCCTGTACGTTGATSNNCCCTTTTCCATAGTA 550 GAA BPN268R AGCTGCCGCCTGTACGTTSNNCAGCCCTTTTCCATA 551 GTA BPN269R CTGAGCTGCCGCCTGTACSNNGATCAGCCCTTTTCC 552 ATA BPN270R TTACTGAGCTGCCGCCTGSNNGTTGATCAGCCCTTT 553 TCC BPN271R GCTTTACTGAGCTGCCGCSNNTACGTTGATCAGCCC 554 TTT BPN272R TAAGCTTTACTGAGCTGCSNNCTGTACGTTGATCAG 555 CCC BPN273R CAGTAAGCTTTACTGAGCSNNCGCCTGTACGTTGAT 556 CAG BPN274R GGCCAGTAAGCTTTACTGSNNTGCCGCCTGTACGTT 557 GAT BPN275R GACGGCCAGTAAGCTTTASNNAGCTGCCGCCTGTAC 558 GTT

BPN′ Multiple Mutation Library Construction

Synthetic BPN′ multiple mutation libraries (or combinatorial libraries) were produced by Geneart, Baseclear, and Woke. Each synthetic BPN′ multiple mutation library contained a mix of BPN′ genes in which two or more selected codons of the mature sequence were randomly replaced by specific DNA sequences. For example: a BPN′ combinatorial library could be designed in such a way that codon 22 of the mature sequence would be randomly substituted for DNA triplets coding for Thr, Gln, Val or Tyr, codon 26 for Val, Gln, Asn or Tyr, codon 31 for Ile, His, Tyr, or Asn and codon 48 for Ala, Glu, His or Asp. In this example, the combinatorial library would contain a maximum of 256 BPN′ combinatorial variants. However, a typical BPN′ multiple mutation library could contain up to thousands of unique BPN′ variant genes. Multiple mutation library fragments having terminal AvaI and HindIII sites (See e.g., wild type BPN′) were digested with AvaI and HindIII, gel-purified and cloned into the pHPLT vector by ligase reaction using Invitrogen® T4 DNA Ligase (Catalog No. 15224-025) as recommended by the manufacturer for general cloning of cohesive ends. The wild type BPN′AvaI/HindIII fragment:

(SEQ ID NO: 559) AAGA

 CGTCGCTTAC GTTGAAGAAG ATCACGTAGC ACATGCGTAC GCGCAGTCCG TGCCTTACGG CGTATCACAA ATTAAAGCCC CTGCTCTGCA CTCTCAAGGC TACACTGGAT CAAATGTTAA AGTAGCGGTT ATCGACAGCG GTATCGATTC TTCTCATCCT GATTTAAAGG TAGCAGGCGG AGCCAGCATG GTTCCTTCTG AAACAAATCC TTTCCAAGAC AACAACTCTC ACGGAACTCA CGTTGCCGGC ACAGTTGCGG CTCTTAATAA CTCAATCGGT GTATTAGGCG TTGCGCCAAG CGCATCACTT TACGCTGTAA AAGTTCTCGG TGCTGACGGT TCCGGCCAAT ACAGCTGGAT CATTAACGGA ATCGAGTGGG CGATCGCAAA CAATATGGAC GTTATTAACA TGAGCCTCGG CGGACCTTCT GGTTCTGCTG CTTTAAAAGC GGCAGTTGAT AAAGCCGTTG CATCCGGCGT CGTAGTCGTT GCGGCAGCCG GTAACGAAGG CACTTCCGGC AGCTCAAGCA CAGTGGGCTA CCCTGGTAAA TACCCTTCTG TCATTGCAGT AGGCGCTGTT GACAGCAGCA ACCAAAGAGC ATCTTTCTCA AGCGTAGGAC CTGAGCTTGA TGTCATGGCA CCTGGCGTAT CTATCCAAAG CACGCTTCCT GGAAACAAAT ACGGGGCGTA CAACGGTACG TCAATGGCAT CTCCGCACGT TGCCGGAGCG GCTGCTTTGA TTCTTTCTAA GCACCCGAAC TGGACAAACA CTCAAGTCCG CAGCAGTTTA GAAAACACCA CTACAAAACT TGGTGATTCT TTCTACTATG GAAAAGGGCT GATCAACGTA CAGGCGGCAG CTCAGTAAGT TAACAGAGGA GGATTTCCT GAAGGAAATC CGTTTTTTTA TTTT

 GGAGA

To transform the ligation reaction mix, the library DNA (BPN′ library fragment mix cloned in pHPLT) was amplified using the TempliPhi kit (Amersham Catalog No. 25-6400). For this purpose, 1 μL of the ligation reaction mix was mixed with 5mL of sample buffer from the TempliPhi kit and heated for 3 minutes at 95° C. to denature the DNA. The reaction was placed on ice to cool for 2 minutes and then spun down briefly. Next, 5mL of reaction buffer and 0.2mL of phi29 polymerase from the TempliPhi kit were added, and the reactions were incubated at 30° C. in an MJ Research PCR machine for 4 hours. The phi29 enzyme was heat inactivated by incubation at 65° C. for 10 minutes.

For transformation of the libraries 0.1 μL of the TempliPhi amplification reaction product was mixed with 500 μL of competent B. subtilis cells (ΔaprE, ΔnprE, oppA, ΔspoIIE, degUHy32, ΔamyE::(xylR,pxylA-comK) followed by vigorous shaking at 37° C. for 1 hour. After this time aliquots of 100 and 500 μL were plated on HI-agar plates containing 20 ppm neomycin and 0.5% skim milk.

The following Table provides a list of some of the single substitutions used in the present invention.

TABLE 3-2 Mutations POS Variant 1 A001T 1 A001V 3 S003F 4 V004M 8 V008I 10 Q010L 10 Q010R 12 K012N 12 K012R 13 A013T 13 A013V 14 P014L 14 P014S 15 A015T 16 L016M 17 H017Q 17 H017R 17 H017Y 19 Q019H 20 G020D 25 N025Y 29 A029V 33 S033G 33 S033I 38 S038F 44 V044I 45 A045V 50 M050I 53 S053F 53 S053T 54 E054D 55 T055I 55 T055S 59 Q059H 59 Q059K 59 Q059L 60 D060N 61 N061D 63 S063T 65 G065R 66 T066G 66 T066I 66 T066S 67 H067R 67 H067S 68 V068C 68 V068D 68 V068G 68 V068I 68 V068L 68 V068N 68 V068S 69 A069G 69 A069S 71 T071G 71 T071I 75 L075G 75 L075I 75 L075R 76 N076D 76 N076G 77 N077Z 79 I079F 81 V081A 81 V081I 84 V084D 84 V084I 85 A085V 86 P086S 86 P086T 88 A088S 88 A088T 88 A088V 92 A092G 92 A092L 92 A092S 92 A092V 93 V093C 93 V093G 93 V093I 93 V093L 93 V093R 93 V093S 94 K094E 94 K094G 94 K094R 94 K094S 94 K094V 94 K094Z 95 V095D 96 L096I 96 L096V 97 G097C 97 G097D 97 G097H 97 G097L 97 G097N 97 G097R 97 G097S 97 G097V 97 G097Y 97 G097Z 98 A098C 98 A098D 98 A098F 98 A098G 98 A098H 98 A098I 98 A098L 98 A098N 98 A098R 98 A098S 98 A098T 98 A098V 98 A098Y 98 A098Z 99 D099C 99 D099F 99 D099G 99 D099H 99 D099I 99 D099L 99 D099N 99 D099R 99 D099S 99 D099V 99 D099Y 99 D099Z 100 G100C 100 G100D 100 G100H 100 G100L 100 G100N 100 G100R 100 G100S 100 G100V 100 G100Z 101 S101C 101 S101D 101 S101F 101 S101G 101 S101H 101 S101I 101 S101L 101 S101N 101 S101P 101 S101R 101 S101V 101 S101Y 101 S101Z 102 G102C 102 G102D 102 G102I 102 G102L 102 G102R 102 G102S 102 G102V 102 G102Z 103 Q103C 103 Q103D 103 Q103F 103 Q103G 103 Q103H 103 Q103I 103 Q103L 103 Q103N 103 Q103R 103 Q103S 103 Q103V 103 Q103Y 103 Q103Z 104 Y104C 104 Y104F 104 Y104G 104 Y104L 104 Y104N 104 Y104R 104 Y104S 104 Y104Z 105 S105G 106 W106C 109 N109D 109 N109S 116 A116D 116 A116G 116 A116H 116 A116T 117 N117C 117 N117G 117 N117H 117 N117I 117 N117L 117 N117R 117 N117S 117 N117V 117 N117Y 117 N117Z 118 N118C 118 N118D 118 N118G 118 N118H 118 N118R 118 N118S 119 M119C 119 M119H 119 M119I 119 M119L 119 M119N 119 M119S 119 M119V 120 D120C 120 D120G 120 D120H 120 D120L 120 D120N 120 D120R 120 D120S 121 V121C 121 V121I 121 V121L 122 I122C 122 I122D 122 I122G 122 I122H 122 I122L 122 I122S 122 I122V 123 N123C 123 N123D 123 N123G 123 N123I 123 N123S 123 N123V 124 M124G 124 M124I 124 M124L 124 M124S 124 M124V 126 L126C 126 L126F 126 L126G 126 L126H 126 L126I 126 L126R 126 L126S 126 L126V 126 L126Y 127 G127C 127 G127D 127 G127H 127 G127L 127 G127N 127 G127R 127 G127S 127 G127V 128 G128C 128 G128D 128 G128H 128 G128N 128 G128R 128 G128S 128 G128Y 129 P129C 129 P129D 129 P129F 129 P129G 129 P129H 129 P129L 129 P129R 129 P129S 129 P129V 129 P129Y 129 P129Z 129 P129R 130 S130C 130 S130D 130 S130F 130 S130G 130 S130H 130 S130I 130 S130L 130 S130N 130 S130R 130 S130V 130 S130Y 130 S130Z 131 G131C 131 G131D 131 G131H 131 G131N 131 G131R 131 G131S 131 G131V 131 G131Y 131 G131Z 132 S132C 132 S132D 132 S132G 132 S132H 132 S132I 132 S132L 132 S132N 132 S132R 132 S132T 132 S132V 132 S132Z 133 A133D 133 A133S 133 A133T 133 A133V 134 A134T 135 L135F 136 K136N 137 A137T 138 A138V 139 V139I 142 A142V 143 V143I 144 A144E 144 A144T 144 A144V 145 S145T 146 G146D 147 V147I 151 A151V 153 A153T 153 A153V 154 G154S 156 E156D 156 E156G 157 G157D 157 G157S 160 G160D 160 G160S 161 S161N 166 G166D 166 G166S 169 G169A 175 I175T 179 A179V 180 V180A 182 S182N 183 S183G 183 S183N 187 A187V 192 V192A 192 V192I 194 P194L 200 A200T 200 A200V 204 S204P 206 Q206R 209 L209F 211 G211V 213 K213E 213 K213N 213 K213R 216 A216E 216 A216T 216 A216V 217 L217S 217 L217Y 218 N218I 228 A228T 230 A230V 231 A231T 233 L233S 236 S236Y 237 K237E 238 H238Q 238 H238Y 241 W241R 243 N243D 244 T244I 244 T244N 244 T244S 245 Q245H 248 S248G 248 S248N 248 S248R 249 S249N 249 S249R 250 L250I 251 E251Q 253 T253I 260 S260F 261 F261L 267 L267G 267 L267M 267 L267R 267 L267V 269 N269D 270 V270I 271 Q271H 272 A272S 273 A273T 273 A273V 275 Q275Z

Preparation of Crude Enzyme Samples Containing BPN′ Variants

The BPN′ variant proteins were produced by growing the B. subtilis transformants in 96 well MTP at 37° C. for 68 hours in MBD medium (a MOPS based defined medium). MBD medium was made essentially as known in the art (See, Neidhardt et al., J. Bacteriol., 119: 736-747 [1974]), except that NH₄Cl₂, FeSO₄, and CaCl₂ were omitted from the base medium, 3 mM K₂HPO₄ was used, and the base medium was supplemented with 60 mM urea, 75 g/L glucose, and 1% soytone. The micronutrients were made up as a 100× stock solution containing in one liter, 400 mg FeSO₄7H₂O, 100 mg MnSO₄.H₂O, 100 mg ZnSO₄7H₂O, 50 mg CuCl₂2H₂O, 100 mg CoCl₂ 6H₂O, 100 mg NaMoO₄ 2H₂O, 100 mg Na₂B₄O₇ 10H₂O, 10 ml of 1M CaCl₂, and 10 ml of 0.5 M sodium citrate.

Example 4 LAS Stability of BPN′ Variants

In this Example, experiments conducted to assess the stability of various single-substitution BPN′ variants and multiple-substitution BPN′ variants in the presence of LAS are described. LAS stability was measured by determining the AAPF activity before and after incubation in the presence of LAS at elevated temperature (45° C.), using the methods described in Example 1. The results of the following tables are shown as relative stability values in which the stability of the variant BPN′ is compared to the wild-type BPN′ enzyme. In particular the relative stability is the ratio of the variant residual activity to the wild-type residual activity. A value of greater than one indicates greater stability in the presence of LAS.

Table 4-1 contains the relative stability values of BPN′ variants as compared to wild-type BPN′. As determined during development of the present invention, numerous BPN′ variants had demonstrably higher stability in the presence of LAS as compared to the wild-type BPN′. In particular in the LAS stability assay of 92 BPN′ sites examined, 40 sites (43%) were poor (deleterious) and 52 sites (57%) were good (beneficial). Moreover of the 1508 variants tested, 96 (6%) were superior (up), 196 (13%) were neutral (same), and 1216 (81%) were inferior (down).

TABLE 4-1 LAS Stability Results for Singly-Substituted BPN′ Variants Variant Variant Variant Code PI Code PI Code PI A1C 2.14 P14T 1.68 P40F 1.43 A1D 2 P14V 1.33 P40H 1.28 A1E 2.06 A15C 2.12 P40I 1.42 A1M 1.37 A15D 2.02 P40L 1.25 A1N 1.57 A15E 2.26 P40Q 1.32 A1Q 1.73 A15P 1.9 P40R 1.77 A1S 1.32 L16I 1.27 P40W 1.68 Q2E 1.22 S18E 2.08 K43A 1.24 S3D 2.5 S18H 1.15 K43C 1.32 S3Q 1.24 S18I 1.24 K43D 1.33 Y6E 1.84 S18M 1.27 K43E 1.26 Y6W 1.56 S18Q 1.12 K43G 1.23 S9C 1.84 S18T 1.13 K43L 1.23 S9E 2.87 S18V 1.28 K43M 1.25 S9G 1.23 S18Y 1.07 K43R 1.1 S9P 2.15 Q19C 1.54 K43S 1.32 S9T 1.28 Q19D 1.81 K43W 1.22 Q10E 1.26 Q19E 1.73 M50I 1.27 I11V 1.37 G20C 1.37 M50K 1.36 K12A 2.13 G20D 1.36 M50K 1.4 K12C 2.49 G20E 1.57 P52K 1.47 K12D 2.11 G20H 1.34 P52R 1.55 K12E 2.47 T22C 1.23 S53E 1.23 K12F 2.49 T22E 1.44 S53K 1.36 K12G 1.87 T22F 1.69 S53R 1.41 K12H 2.29 T22L 1.21 N56D 1.29 K12I 2.38 T22W 1.52 F58C 1.24 K12N 2.56 T22Y 1.68 Q59C 1.32 K12Q 2.15 N25E 1.35 Q59D 1.51 K12S 2.13 N25F 1.24 Q59E 1.43 K12T 1.78 N25W 1.27 Q59N 1.13 K12V 2.3 K27G 1.22 H67P 2.06 K12W 2.12 K27P 1.64 S78C 1.8 K12Y 2.41 I35A 1.56 S78D 1.69 P14C 2.23 I35C 1.53 S78F 1.39 P14D 2.89 I35S 1.23 S78I 1.28 P14E 2.55 I35T 1.63 S78K 1.61 P14G 1.11 I35V 1.5 S78L 1.21 P14I 1.37 S37E 1.22 S78N 1.28 P14L 1.44 S37R 1.89 S78Q 1.26 P14N 1.72 P40C 1.6 S78R 2.52 P14S 1.36 P40E 1.86 S78W 1.41 S78Y 1.21 W106G 1.36 M124I 1.93 I79E 1.76 W106H 1.29 M124L 1.29 P86Y 1.31 W106I 1.42 L126I 1.69 S89C 1.26 W106L 1.59 L126V 1.51 S89D 1.26 W106M 1.39 L126W 1.26 S89G 1.24 W106R 1.48 G128A 1.84 Y91I 1.29 W106S 1.42 G128S 1.63 Y91V 1.28 W106T 1.59 G131P 1.52 L96I 1.3 W106V 1.23 G131R 1.22 L96V 1.32 W106Y 1.38 A133C 1.7 A98C 1.41 N109C 1.42 A133D 1.88 A98D 1.3 N109F 2.04 A133E 1.61 A98I 1.2 N109H 1.36 A133F 1.37 A98S 1.1 N109L 1.84 A133I 1.23 A98T 1.08 N109P 1.5 A133L 1.33 D99R 1.25 N109Q 1.18 A133P 1.62 S101C 1.29 N109R 2.25 A133R 1.83 S101E 1.4 N109V 1.56 A133W 1.34 S101G 1.61 N109W 1.65 A134D 1.4 S101P 1.19 N109Y 1.22 A134E 1.47 G102A 1.42 E112A 2.9 A134G 1.22 G102S 1.27 E112C 2.08 K136E 2.28 Q103C 1.39 E112F 2.75 K136H 1.41 Q103F 1.42 E112G 2.84 A137C 1.22 Q103G 1.65 E112I 2.85 A137F 1.86 Q103I 1.4 E112L 2.68 A137H 1.27 Q103K 1.63 E112M 2.86 A137K 1.55 Q103M 1.22 E112N 1.98 A137L 1.35 Q103N 1.25 E112Q 2.53 A137M 1.25 Q103R 1.58 E112S 2.68 A137R 2.01 Q103T 1.5 E112T 2.56 A137W 1.92 Q103W 1.69 E112V 2.59 A137Y 1.51 S105A 1.29 E112W 2.84 V139C 2.09 S105C 1.27 E112Y 2.53 K141C 1.54 S105D 1.46 W113N 1.22 K141D 1.31 S105E 1.38 I115N 1.45 K141E 1.29 S105K 1.89 I115R 1.7 K141F 1.5 S105L 1.25 I115T 1.31 K141G 1.44 W106A 1.31 A116D 1.23 K141H 1.58 W106C 1.53 A116K 1.55 K141I 1.54 W106E 1.69 A116R 1.62 K141L 1.46 W106F 1.43 N118C 1.23 K141N 1.43 K141Q 1.39 S183C 1.92 Y217L 1.54 K141S 1.28 S183E 2.48 Y217M 2.3 K141W 1.64 S183N 1.82 Y217N 1.26 K141Y 1.28 S183Q 1.46 Y217Q 1.55 V143D 1.28 N184C 1.61 Y217R 1.26 V143E 1.37 Q185C 1.65 N218C 1.29 A144C 1.52 Q185E 2.41 N218S 2.38 A144D 1.58 S188C 1.52 N218T 1.45 A144E 1.47 S188D 2.58 S224C 1.61 A144I 1.24 S188E 2.55 P225A 2.82 A144K 1.59 S188P 1.36 P225C 1.43 A144L 1.29 P194C 1.5 P225G 2.86 A144R 2.42 P194E 1.73 P225I 1.69 A144W 1.8 Q206C 1.91 P225S 2.39 S145C 1.41 Q206D 2.47 P225V 2.14 S145D 1.26 Q206E 2.77 G229A 1.59 S145E 1.27 Q206L 1.23 A230G 1.29 S145F 1.29 Q206M 1.23 I234V 1.26 S145L 1.26 Q206W 1.39 L235G 1.46 S145M 1.36 Q206Y 1.43 L235I 1.54 S145R 1.65 N212C 1.22 L235K 1.21 E156C 1.3 N212E 1.51 L235M 1.58 E156Y 1.26 K213A 2.14 L235N 1.39 T158D 1.8 K213C 2.29 L235Q 1.63 T158E 2.16 K213D 2.59 L235S 1.51 T158V 1.31 K213E 2.44 L235W 1.92 S159C 1.84 K213H 1.72 L235Y 1.95 S159D 1.68 K213I 1.3 S236E 1.35 S159Q 1.22 K213L 1.58 S236H 1.29 S162C 1.77 K213M 2.1 H238F 1.42 S162E 2.1 K213N 2.21 P239N 1.22 S162M 1.31 K213Q 2.12 P239T 1.32 S162N 1.45 K213S 2.34 P239V 1.26 S162Q 1.52 K213T 2.31 T244D 1.47 G169A 2.88 K213V 1.3 T244F 1.3 K170A 1.54 A216C 2.07 T244H 1.45 P172E 2.3 A216D 2.09 T244K 1.29 P172R 1.23 A216E 2.62 T244R 1.73 A176C 2 Y217C 2.31 Q245C 1.31 S182C 1.64 Y217D 1.46 Q245D 1.37 S182D 2.02 Y217E 2.11 Q245E 1.32 S182Q 1.39 Y217K 1.42 S248E 1.47 N252C 1.36 K256M 2.23 K265C 1.92 N252E 1.81 K256N 2.5 K265E 1.83 T254A 2.1 K256P 2.82 K265H 2.28 T254C 2.32 K256Q 2.3 K265L 1.38 T255C 1.24 K256S 2.23 K265M 1.48 T255D 1.54 K256T 2.22 K265N 2.19 T255E 2.29 K256V 2.4 K265Q 2.1 K256A 2.61 K256W 2.79 K265S 1.49 K256C 2.44 K256Y 2.71 K265Y 1.7 K256D 2.81 S260C 1.25 N269D 1.95 K256E 2.81 S260D 1.86 Q271C 1.53 K256F 2.4 S260E 2.6 Q271D 1.86 K256H 2.42 S260P 2.49 Q271E 2.24 K256I 2.37 K265A 1.71 A272E 1.5 K256L 1.99 S101Y 1.26 G166S 2.41 V008I 1.41 G102A 1.41 G169A 1.59 T022E 1.62 G102S 1.57 K170A 1.26 T022F 1.57 Q103A 1.18 K170E 1.58 T022M 1.23 Q103C 1.67 V203C 1.19 T022S 1.18 Q103E 1.48 S101Q 1.19 T022W 1.65 Q103F 1.47 S101T 1.21 T022Y 1.69 Q103I 1.3 S101V 1.55 V0026F 1.18 Q103L 1.2 G166N 2.21 V0026G 1.18 Q103S 1.2 G166Q 2.53 I031E 1.25 Q103T 1.26 G166R 1.63 I031F 1.17 Q103V 1.18 S101I 1.17 I031H 1.24 Q103W 1.34 S101L 1.28 I031N 1.23 Y104F 1.28 S101N 1.17 I031S 1.2 Y104W 1.58 G166H 2.19 I031T 1.32 M124I 2.02 G166K 1.17 A0045E 1.28 V147A 1.17 G166M 2.65 H067P 1.32 V147E 1.26 G097E 1.2 V072A 1.38 V147S 1.35 S101C 1.25 V072C 1.25 V149A 1.82 S101E 1.42 S087D 1.32 V149C 1.43 V149S 1.49 A092S 1.22 V149D 1.39 V149T 1.22 L096I 1.39 V149E 2.06 G166C 2.3 L096M 1.34 V149F 1.68 G097D 1.43 V149P 1.23

TABLE 4-2 LAS Stability Results for Multiply-Substituted BPN′ Variants Variant Code PI S024S-V028V-M050M-A092A-Q103E-A114G-V246V 1.21 S024S-V028V-M050V-A092A-Q103Q-A114A-V246V 1.10 S024S-V028V-M050V-A092A-Q103Q-A114G-V246V 1.22 S024H-V028V-M050V-A092A-Q103Q-A114A-V246T 1.20 S024H-V028V-M050V-A092A-Q103E-A114A-V246V 1.24 S024H-V028V-M050V-A092A-Q103Q-A114G-V246V 1.18 S024H-V028V-M050M-A092A-Q103E-A114A-V246V 1.11 S024H-V028V-M050M-A092A-Q103E-A114A-V246T 1.22 S024S-V028V-M050M-A092G-Q103Q-A114A-V246T 1.11 S024H-V028V-M050M-A092A-Q103Q-A114G-V246T 1.14 S101E-M119N-K213N 1.65 S101N-K213I 1.22 S101N-M119H 1.12 M119H-K213I-Y217L 1.43 S101N-M119H-K213N-Y217L 1.53 S101N-K213L-Y217E 1.79 M119N-K213N-Y217L 1.71 M119F-K213L-Y217E 1.62 S101P-K213N 1.64 S101N-M119H-K213N 1.63 S101N-M119F-K213I-Y217L 1.43 K213L 1.38 M119N-K213N 1.70 K213N 1.51 K213I-Y217E 1.36 S101N-M119H-Y217Q 1.41 S101P-K213N-Y217L 1.66 M119N-K213I 1.25 K213N-Y217Q 1.66 M119H-K213N 1.62 S101N-K213L-Y217Q 1.49 S101P-K213N 1.66 S101E-K213N-Y217E 1.81 S101E-M119H-K213I-Y217Q 1.52 S101E-M119H-K213N 1.65 K213I-Y217Q 1.27 S101N-K213I-Y217Q 1.53 M119H-Y217Q 1.39 S101N-M119N-K213N-Y217Q 1.89 M119H-K213I-Y217Q 1.44 K213I-Y217Q 1.24 S101E-M119N-Y217L 1.45 M119F-K213L 1.34 M119H-K213N-Y217E 1.91 S101N-M119N-K213N-Y217Q 1.75 S101N-M119H-K213N-Y217Q 1.75 M119H-K213I-Y217Q 1.93 Y217Q 1.18 M119H-K213N-Y217Q 1.73 S101N-M119F-Y217E 1.39 M119F-Y217Q 1.17 S101N-M119F-K213I-Y217Q 1.22 S101N-K213I-Y217L 1.19 S101N-M119H-K213N-Y217L 1.44 S101E-K213L-Y217L 1.54 S101N-K213N-Y217Q 1.45 S101N-M119H-K213L 1.29 S101N-M119H-K213I 1.22 S101P-K213N-Y217L 1.46 M119F-K213I-Y217Q 1.24 S101N-K213I-Y217Q 1.24 S101E-M119H-K213I-Y217L 1.92 S101N-M119H-K213I-Y217Q 1.58 M119H-K213N-Y217E 1.49 S101N-M119N-K213N-Y217L 1.46 A048E-K213L 1.28 A048H-K213L 1.25 V026Q-A048Y-K213L 1.19 K213N 1.34 V026N-K213L 1.24 V026N-K213L 1.23 V026Y-K213N 1.44 A048D-K213N 1.22 V026Q-A048E-K213L 1.24 A048H-K213N 1.34 V026Q-A048H-K213L 1.24 A048H-K213L 1.28 K213L 1.25 K213N 1.51 V147D-K213L 1.31 K213I 1.10 V026Q-A048E-K213N 1.28 V026N-A048E-K213N 1.48 A048E-K213L 1.92 V026Y-A048E-K213I 1.71 A048D-K213N 1.46 K213I 1.10 A048H-K213N 1.54 V147D-K213N 1.54 Y021H-A045V-S101E-Y217L 1.21 Y021H-Y217L 1.15 Y021H-A045V-S101E-Y217Q 1.29 Y021H-A045I-S101E-Y217L 1.20 Y021H-Y217Q 1.14 Y021H-A045V-Y217E 1.36 A045V-Y217L 1.14 Y021H-A045V-S101N-Y217Q 1.25 Y021W-S101P-Y217L 1.13 Y021W-A045I-Y217E 1.32 Y021H-A045V-S101E-Y217E 1.50 Y021H-A045I-S101E-Y217L 1.25 Y021H-A045I-S101E-Y217Q 1.36 Y021H-A045V-Y217E 1.31 Y021W-S101E-Y217L 1.27 S101E-Y217L 1.32 Y021H-A045V-Y217Q 1.19 Y021H-Y217E 1.46 Y021W-Y217E-(N0212S) 1.24 A045I-Y217Q 1.15 Y021H-A045V-Y217E 1.43 Y021W-A045V-S101E-Y217Q 1.25 Y021H-S101E-Y217E 1.49 Y021W-S101N-Y217L 1.16 S024S-V028V-M050M-A092A-Q103Q-A114A-V246T 1.17 Y021H-A045V-S101E 1.15 Y021W-A045V-S101E-Y217L 1.25 S101N-M119H-K213K-Y217Q 1.38 S101S-M119N-K213N-Y217Q 1.68 Y021H-A045V-S101P-Y217L 1.23 S024S-V028V-M050M-A092A-Q103Q-A114G-V246T 1.29 S101S-M119F-K213I-Y217Q 1.34 S101S-M119M-K213K-Y217L 1.35 Y021H-A045I-S101E-Y217Q 1.32 Y021H-A045V-S101E-Y217E 1.57 Y021H-A045V-S101E 1.19 Y021H-Y217L 1.18 Y021H-A045I-Y217E 1.54 Y021W-A045I-S101E-Y217E 1.47 S101N-M119F-K213K-Y217L 1.26 S101E-M119H-K213N-Y217E 1.37 Y021H-A045I-Y217E 1.44 S101S-M119H-K213L-Y217L 1.56 Y021H-Y217E 1.67 S101S-M119F-K213K-Y217Q 1.25 Y021H-A045I-S101E-Y217L 1.46

Example 5 Specific Activity of BPN′-Variants

In this Example, experiments conducted to determine the relative specific activity of BPN′ and BPN′-variants is described. Specific activity towards AAPF was measured using methods provided in Example 1. In Table 5-1, results are shown as relative specific activity values in which the activity of BPN′ variants is compared to activity of wild-type BPN′. In particular the relative specific activity is the ratio of the variant specific activity to the wild-type specific activity. A value greater than one (PI>1) indicates higher specific activity towards the AAPF substrate.

TABLE 5-1 Specific Activity of Singly-Substituted BPN′ Variants Variant Variant Variant Code PI Code PI Code PI Y006N 1.25 I115R 1.30 I175V 2.81 Y006T 1.21 G131P 1.29 Y217C 1.33 Q019E 1.26 G131R 1.21 Y217L 3.96 I035T 1.17 A137W 1.18 Y217M 1.85 L042V 1.19 A137Y 1.18 Y217S 1.48 M050K 1.32 V139C 1.23 N218S 1.22 M050R 1.51 K141F 1.18 S236V 1.21 M050T 1.35 K141I 1.39 H238R 1.46 Q059W 1.59 K141S 1.19 K256F 1.17 P086M 1.44 K141Y 1.25 K256P 1.26 P086Y 1.22 V143D 1.21 K256Q 1.32 A098I 1.26 V143N 1.35 K256W 1.20 A098T 1.34 V143Q 1.41 K256Y 1.27 A098V 1.49 S145M 1.25 N109Q 1.19 S145R 1.36 N109T 1.28 G146M 1.39 N109V 1.45 K170A 1.32

Example 6 Comparative Evaluation of BPN′-Variant Data

In this Example, results of experiments conducted to determine protein expression, stain removal activity, LAS stability, and AAPF activity (tests of properties of interest) of BPN′ and BPN′-variants are described. The results were obtained using the methods described in Example 1. As described throughout, functionality of the BPN′ variants was quantified as a performance index (PI), which is the ratio of performance of a variant to a parent protein. PI gradations used herein include: Up mutations (PI >1.0); Neutral mutations (PI>0.5); Non-deleterious mutations (PI>0.05); and Deleterious mutations (PI≦0.05). “Combinable mutations” are those mutations for which the variant has Performance index values=0.5 for at least one property, and >0.05 for all properties. Combinable mutations are mutations that can be combined to deliver proteins with appropriate Performance indices for one or more desired properties. Positions at which mutations occur are classed as follows: Non-restrictive positions have ≧20% neutral mutations for at least one property; and Restrictive positions have <20% neutral mutations for activity and stability.

These data find use in engineering any subtilisin. Even if the subtilisin to be engineered has an amino acid different from that of subtilisin BPN′ at a particular position, this data find use in identifying at least one substitution that will alter the desired properties by identifying the best choice substitution, including substitution to the BPN′ wild type amino acid.

Table 6-1 provides Performance index values (Pi) for 5,004 variants of subtilisin BPN′ at 275 positions. Performance indices less than or equal to 0.05 were fixed to 0.05 and indicated in bold italics in the table. Also, for the stability measure, if the Performance index of activity in the stability assays was less than or equal to 0.05, the associated stability performance index was fixed to 0.05.

TABLE 6-1 Performance Index Values for BPN′ Variants PI PI BMI PI BMI BMI LAS- Posi- BPN′ TCA pH 8 pH 7 pH 8 EDTA AAPF tion variant PI 16 C. 16 C. 32 C. PI PI 1 A001C 0.74 0.84 1.10 0.79 1.1 0.87 1 A001D 1.34 0.93 1.12 0.88 1.1 0.88 1 A001E 0.82 0.94 0.85 0.84 1.5 0.94 1 A001F 1.39 0.94 1.01 0.84 0.4 0.90 1 A001G 1.39 0.90 1.12 1.06 1.1 1.04 1 A001H 1.26 0.99 1.04 0.98 0.9 0.97 1 A001I 1.50 0.72 1.00 0.92 0.6 0.88 1 A001K 1.23 0.83 0.79 1.11 0.2 0.96 1 A001L 0.96 0.86 0.81 0.94 0.6 0.94 1 A001M 1.34 1.02 1.07 1.08 0.9 0.99 1 A001N 1.29 1.02 0.81 0.98 1.0 1.05 1 A001P 0.27 1.16 1.46 1.14 0.7 0.66 1 A001Q 0.88 1.00 0.97 0.98 1.2 1.02 1 A001R 1.00 0.89 0.72 0.91 0.1 1.00 1 A001S 1.09 0.89 1.00 1.05 0.9 1.08 1 A001T 1.13 1.00 1.16 1.02 1.0 1.01 1 A001V 1.32 0.83 0.68 0.96 0.8 0.96 1 A001W 1.19 0.76 0.67 0.88 0.2 0.92 1 A001Y

2 Q002A 0.78 0.88 0.99 1.01

0.94 2 Q002C 0.55 0.81 1.26 0.92 0.1 0.74 2 Q002D 1.01 0.94 0.96 1.02

0.96 2 Q002E 1.18 0.87 1.01 0.79

0.85 2 Q002F 0.44 1.18 0.91 0.97

0.78 2 Q002G 0.80 1.11 0.31 1.02

0.71 2 Q002H

2 Q002I 0.37 1.16 0.99 1.08

0.77 2 Q002K 0.40 1.02 0.75 1.03

0.86 2 Q002L 0.34 0.90 1.24 1.15

0.70 2 Q002M 0.47 0.96 0.92 0.92

0.79 2 Q002N

2 Q002P 0.76 0.84 0.82 1.12

0.94 2 Q002R 0.35 0.79 0.84 1.11

0.78 2 Q002S 0.77 0.93 1.23 0.80

0.88 2 Q002T 0.38 0.93 0.95 0.93

0.82 2 Q002V 0.42 1.17 0.96 1.17

0.86 2 Q002W 0.17 3.77 6.93 2.44

0.47 2 Q002Y 0.44 0.93 0.85 1.03

0.86 3 S003A 1.19 1.20 0.97 0.89 0.3 0.93 3 S003C

3 S003D 1.24 1.11 1.08 0.97 1.0 1.02 3 S003E

3 S003F 1.20 0.90 0.95 0.86 0.2 1.02 3 S003G 1.45 0.96 1.03 1.05

0.91 3 S003H

3 S003I 1.24 0.80 0.90 1.05 1.0 0.92 3 S003K 1.28 0.97 0.80 0.95 0.1 1.09 3 S003L 1.13 0.90 0.84 1.06 0.6 0.92 3 S003M 1.35 0.83 1.04 0.92 1.1 0.84 3 S003N 1.18 0.98 1.15 0.85 0.5 1.01 3 S003P 1.01 1.08 1.09 0.89

0.90 3 S003Q 1.38 0.97 0.96 1.08 1.3 1.00 3 S003R 1.37 0.75 0.62 1.00

0.98 3 S003T 1.31 1.09 1.01 0.87 1.2 0.90 3 S003V 1.19 0.84 0.80 1.06 1.0 0.99 3 S003W 1.50 0.71 0.65 0.91 0.1 0.84 3 S003Y 1.25 0.76 0.72 0.92 0.2 0.88 4 V004A 0.83 0.90 1.07 1.00

0.95 4 V004C 0.87 1.03 1.22 0.92 0.3 1.09 4 V004D 0.78 0.87 1.06 0.98

0.91 4 V004E 1.00 1.04 1.22 0.92 0.1 0.99 4 V004F

4 V004G 0.45 0.86 1.15 1.14

0.78 4 V004H

4 V004I

4 V004K 0.89 0.83 1.01 1.08

1.24 4 V004L 1.07 0.97 1.12 0.94

1.13 4 V004M 1.14 1.06 1.03 0.98

0.87 4 V004N 0.98 1.22 1.02 1.09

0.93 4 V004P 0.75 1.19 1.16 0.92

1.00 4 V004Q 0.91 0.85 1.16 0.78

1.30 4 V004R 1.01 0.83 0.90 0.85

1.20 4 V004S 0.80 0.91 1.14 0.77

1.00 4 V004T 1.02 0.92 1.27 0.97 1.2 1.20 4 V004W 0.93 0.99 0.92 0.99

1.16 4 V004Y 0.79 0.93 1.03 1.08

0.89 5 P005A 0.53 0.86 0.73 0.79

0.60 5 P005C 0.70 0.94 0.80 0.92

0.60 5 P005D

5 P005E 0.79 1.02 0.79 0.94

0.84 5 P005F 0.22 0.55 0.44 0.61 0.1 0.23 5 P005G 0.98 1.09 1.10 0.98 0.3 1.13 5 P005H 0.38 0.96 0.88 1.09

0.64 5 P005I 0.21 0.49 0.96 1.02 0.1 0.20 5 P005K 0.16 4.53 2.60 0.65 0.6 0.06 5 P005L 0.21 1.50 1.40 1.49

0.47 5 P005M 0.41 1.02 1.11 1.13

0.84 5 P005N 0.68 0.91 0.91 1.00

0.78 5 P005Q 0.70 1.08 0.84 0.97

0.60 5 P005R 0.16

1.56 0.3 0.07 5 P005S 0.74 0.98 1.09 1.01

0.81 5 P005T 0.73 1.16 0.91 0.97

1.46 5 P005V 0.27 0.72 1.30 1.14

0.73 5 P005W 0.43 0.79 0.82 0.76

0.60 5 P005Y 0.17 3.33 3.27 2.19

0.35 6 Y006A 1.02 1.14 1.03 1.01 0.8 0.97 6 Y006C 1.04 1.03 0.95 0.83 0.7 0.91 6 Y006D

6 Y006E 1.49 1.13 0.76 1.00 1.1 0.81 6 Y006F 1.17 0.84 0.88 0.81 0.6 0.92 6 Y006G 1.00 1.20 1.09 0.78 0.7 0.86 6 Y006H

6 Y006I

6 Y006K 1.36 0.90 0.70 0.92

0.91 6 Y006L 0.15

0.7 0.16 6 Y006M 1.31 1.16 1.04 0.96 0.6 0.86 6 Y006N 1.12 1.20 0.97 0.81 0.6 0.93 6 Y006P 0.92 1.10 0.77 0.96 0.7 1.13 6 Y006Q 1.36 1.29 1.19 0.87 0.9 0.94 6 Y006R 0.75 0.76 0.61 0.93

0.92 6 Y006S 0.83 1.08 1.20 0.96 0.5 0.96 6 Y006T 1.13 1.02 1.14 1.12 0.7 0.85 6 Y006V 1.39 1.02 0.97 0.91 0.7 1.06 6 Y006W 1.96 1.06 1.00 0.96 1.1 0.82 7 G007A 0.73 0.88 0.77 1.07

0.60 7 G007C 0.20 0.75 0.37 1.11 0.2 0.08 7 G007F 0.22 0.08

7 G007I 0.34 0.06

7 G007K 0.35 0.11

7 G007L 0.37

7 G007M 0.27

7 G007N 0.95 0.85 0.85 0.95

0.66 7 G007Q 0.15

7 G007R 0.25 0.16

7 G007S 0.85 0.72 0.70 0.96

0.67 7 G007T 0.19 2.98 2.43 3.02 0.1 0.21 7 G007V 0.34

7 G007W 0.16

4.88

7 G007Y 0.20 0.39

8 V008A 0.57 1.02 0.78 0.98

0.69 8 V008C 0.81 0.87 0.93 1.10 0.1 0.83 8 V008D 0.27

8 V008F 0.46 0.77 0.76 1.07

0.70 8 V008G 0.26 1.38 0.49 1.41

0.41 8 V008H 0.39 0.88 0.66 1.25

0.43 8 V008I 0.91 1.06 0.87 1.01 1.0 0.93 8 V008K 0.19 3.07 3.04 3.06 0.2 0.45 8 V008L 0.83 0.91 0.98 1.03 0.2 0.80 8 V008M 0.85 0.95 0.98 0.92

0.74 8 V008P 0.19 2.71 3.00 2.94

0.55 8 V008Q 0.30 0.94 0.74 1.43

0.63 8 V008R 0.21 0.83 0.14 1.14 0.2 0.06 8 V008S 0.30 1.14 0.89 1.37

0.62 8 V008T 0.74 0.76 0.69 1.10

0.79 8 V008Y 0.13

0.3 0.07 9 S009A 1.22 0.84 1.00 0.98 0.8 0.97 9 S009C 1.32 0.94 0.80 0.79 1.2 1.15 9 S009D 0.43

9 S009E 1.89 0.91 0.76 0.92 1.5 0.91 9 S009F 1.43 1.06 0.79 1.04

0.96 9 S009G 1.19 0.88 0.92 0.88 0.7 0.91 9 S009H 1.35 0.70 1.08 1.00 0.8 0.95 9 S009I

9 S009K 0.96 0.76 0.66 0.95

1.13 9 S009L 1.30 0.99 0.76 0.86 0.6 1.05 9 S009M 1.32 0.98 0.95 0.99 0.8 1.17 9 S009N

9 S009P 1.38 1.00 0.87 0.94 0.7 1.06 9 S009Q 1.02 0.92 0.77 0.83 0.8 1.15 9 S009R 1.21 0.98 0.82 0.77

0.98 9 S009T 1.16 1.07 1.11 0.80 1.3 0.94 9 S009V 1.51 0.99 0.75 0.86 0.9 1.03 9 S009W 1.31 0.86 0.84 0.82

1.34 9 S009Y

10 Q010A 1.06 0.90 1.06 1.00 0.5 0.87 10 Q010C 1.25 0.92 0.94 0.93 0.7 0.86 10 Q010D

10 Q010E 1.07 0.70 1.01 0.99 1.5 0.79 10 Q010F 1.18 0.89 0.84 0.98

1.10 10 Q010G 1.34 0.95 0.93 0.90 0.3 1.29 10 Q010H 1.20 1.04 1.07 0.92 0.9 1.29 10 Q010I 1.22 0.80 0.70 0.72

0.75 10 Q010K 1.16 0.83 0.49 0.89 0.1 0.96 10 Q010L 1.19 0.89 0.68 0.85

0.91 10 Q010M 1.26 0.82 0.97 1.07 0.5 0.90 10 Q010N

10 Q010P 0.18

1.50 0.09

10 Q010R 1.15 0.82 0.60 0.73

0.95 10 Q010S 1.00 0.88 0.90 0.87 0.5 1.10 10 Q010T 1.25 1.04 1.00 0.85 0.8 0.93 10 Q010V 1.24 0.96 0.80 1.00 0.2 1.18 10 Q010W 1.04 0.97 0.81 1.00

0.97 10 Q010Y 0.44 0.97 0.79 0.99 0.4 0.82 11 I011A 0.28 0.90 1.10 1.10 0.3 0.65 11 I011C 1.02 1.07 0.88 0.90 0.7 1.00 11 I011D 0.34

11 I011E 0.17

0.53

11 I011F

11 I011G 0.18 2.21 2.17 1.57 0.4 0.27 11 I011H 0.16 36.45  114.23  1.88 0.8 0.35 11 I011K 0.34

0.07

11 I011L 0.76 1.07 1.13 0.79 0.6 1.15 11 I011M

11 I011N 0.28

11 I011P 0.28

0.07

11 I011Q 0.14

11 I011R 0.30

11 I011S 0.26 1.34 1.73 1.26 0.3 0.97 11 I011T 1.05 1.02 0.87 0.93 0.7 1.00 11 I011V 1.28 1.17 0.91 0.86 1.0 1.10 11 I011W 0.30

0.07

11 I011Y 0.21

0.11

12 K012A 1.48 0.85 0.82 1.02 1.2 0.84 12 K012C 1.24 0.73 0.94 0.93 1.4 0.94 12 K012D 1.26 0.49 1.06 0.89 1.4 0.96 12 K012E 1.35 0.62 0.71 0.85 1.4 0.90 12 K012F 1.04 0.60 0.80 0.68 1.3 0.94 12 K012G 1.50 0.94 0.88 0.90 1.4 0.88 12 K012H 1.24 0.94 1.03 0.92 1.3 1.01 12 K012I 1.24 0.68 0.65 0.96 1.2 0.92 12 K012L 0.17 3.09 4.59 1.99 0.6 0.28 12 K012M 0.34

0.06

12 K012N 1.13 0.86 0.93 0.85 1.3 1.01 12 K012P 0.31

12 K012Q 1.35 0.96 0.61 1.01 1.3 1.10 12 K012R 0.73 0.83 0.84 0.83 0.9 0.75 12 K012S 1.07 0.71 0.74 0.72 1.0 0.93 12 K012T 1.13 1.07 0.95 0.84 1.1 0.85 12 K012V 1.57 0.80 0.83 0.98 1.1 0.76 12 K012W 1.35 0.54 0.85 0.94 1.2 0.90 12 K012Y 1.38 0.52 0.90 0.67 1.3 0.95 13 A013C 1.05 0.99 0.77 0.83 0.6 1.12 13 A013D

13 A013E 0.35

13 A013F 0.33

0.08

13 A013G 1.56 1.02 1.05 0.84 0.7 0.92 13 A013H 0.33

13 A013I 0.19 1.12 1.48 1.44

0.31 13 A013K 0.37

13 A013L 0.26 1.12 1.04 1.19 1.1 0.80 13 A013M 0.16 1.38

0.81

13 A013N

13 A013P 0.19 0.15

0.07

13 A013Q 0.15 0.17

13 A013R 0.30

0.07

13 A013S 0.91 1.05 1.10 1.05 1.1 1.23 13 A013T 0.51 1.12 0.91 0.96 0.6 0.82 13 A013V 0.82 1.01 0.74 0.97 0.1 0.76 13 A013W 0.27

0.07

13 A013Y

14 P014A 1.21 0.97 1.13 1.04 0.1 1.07 14 P014C 1.05 0.78 1.22 0.84 0.7 0.99 14 P014D 1.07 0.70 1.21 0.92 0.4 1.02 14 P014E 1.27 0.55 1.14 0.95 0.9 1.14 14 P014F 0.93 0.57 0.89 0.90

1.07 14 P014G 1.35 0.92 1.20 0.94 0.2 1.18 14 P014H

14 P014I 0.89 0.85 1.19 0.94 0.7 1.19 14 P014K 1.36 0.51 0.90 0.95

1.01 14 P014L 0.43 0.74 1.58 1.02 0.6 1.16 14 P014M 1.50 0.77 1.17 0.93 0.3 1.08 14 P014N 1.10 0.80 0.98 0.91 0.1 1.00 14 P014Q 1.34 0.62 0.94 0.81 0.6 1.12 14 P014R 1.19 0.41 0.67 0.98

1.15 14 P014S 0.96 0.79 1.06 0.96 0.1 1.13 14 P014T 0.98 0.99 1.08 0.83 0.9 1.35 14 P014V 1.32 0.88 1.10 0.90 0.7 1.12 14 P014W 1.17 0.84 1.18 0.94

0.92 14 P014Y 1.16 0.92 0.95 1.01

0.93 15 A015C 1.72 0.83 0.87 0.90 1.3 0.83 15 A015D 1.60 0.66 0.77 0.75 1.3 1.00 15 A015E 1.68 0.62 0.77 1.11 1.5 0.87 15 A015F 1.39 0.78 0.68 0.85 0.9 0.99 15 A015G 1.63 0.77 0.66 0.76 0.9 0.79 15 A015H 0.90 0.64 0.77 0.93 1.0 1.01 15 A015I 1.52 0.46 0.88 0.86 1.1 0.95 15 A015K 1.50 0.74 0.59 0.69 0.3 0.98 15 A015L 1.52 0.89 0.77 0.88 1.1 0.85 15 A015M 0.96 0.95 0.62 1.01 1.0 0.99 15 A015N

15 A015P 1.41 0.57 0.64 0.73 0.9 0.95 15 A015Q 1.39 0.55 0.73 1.05 1.1 1.06 15 A015R 1.44 0.67 0.53 0.84 0.1 0.95 15 A015S 1.17 0.74 0.80 1.07 0.9 1.08 15 A015T 1.53 0.85 0.68 0.93 1.0 1.00 15 A015V 1.50 0.77 0.73 0.89 1.0 0.93 15 A015W 0.45 0.59 0.88 1.18 0.8 0.93 15 A015Y 1.43 0.63 0.70 0.90 1.0 0.94 16 L016A 1.14 0.79 1.22 0.96 0.8 0.84 16 L016C 1.01 0.71 1.15 1.08 1.0 1.13 16 L016D 0.20

0.39 0.36 0.3 0.09 16 L016E 1.02 0.57 1.18 1.09 0.9 1.03 16 L016F 0.45 0.63 0.93 0.89 0.5 0.58 16 L016G 0.29 0.54 1.19 0.97 0.8 0.47 16 L016H 0.29 0.70 1.11 1.12 0.5 0.53 16 L016I 1.22 0.51 1.21 1.05 1.0 0.89 16 L016K 0.36 0.62 1.09 0.99 0.5 0.73 16 L016M 1.63 0.76 0.97 1.13 1.0 0.89 16 L016N 0.59 0.71 1.10 1.05 0.8 0.96 16 L016P 0.50 0.73 1.05 1.07 0.8 0.90 16 L016Q 0.90 0.88 1.02 1.04 0.9 0.88 16 L016R 0.15

0.21 16 L016S 0.92 0.81 1.09 0.96 0.7 0.82 16 L016T 1.30 0.63 1.02 1.07 0.9 0.93 16 L016V 0.17

1.28 0.30

16 L016W 0.17 3.37 6.22 3.16 0.1 0.35 16 L016Y 0.25 0.76 1.58 1.43

0.47 17 H017A 0.37 0.41 0.95 0.94 0.4 0.40 17 H017C 0.33 0.80 0.73 1.01 0.7 0.39 17 H017D 0.18

0.22 0.26

17 H017E 0.30 0.81 1.09 1.00 0.4 0.63 17 H017F 1.40 0.72 1.01 0.85 0.3 0.86 17 H017G 0.19 1.02 0.45 1.57 0.6 0.25 17 H017I 1.36 0.57 0.99 1.10 0.8 0.94 17 H017K 0.13

0.2 0.10 17 H017L 1.15 0.90 1.06 0.93 0.5 0.82 17 H017M 1.29 0.60 1.24 0.94 0.7 0.84 17 H017N

17 H017P 0.14

17 H017Q

17 H017R 0.15

0.11 17 H017S 0.20 1.15 1.18 1.54 0.4 0.34 17 H017T 0.47 0.97 1.25 1.13 0.2 0.89 17 H017V 0.80 0.67 0.96 1.02 0.4 0.67 17 H017W 1.54 0.60 1.13 1.03

1.07 17 H017Y 0.49 0.77 1.33 1.06

0.67 18 S018A 0.89 0.57 1.16 0.91 0.9 0.95 18 S018C

18 S018D 1.72 0.78 1.03 0.86 0.8 0.86 18 S018E 1.65 0.75 1.15 0.99 1.3 0.85 18 S018F 1.74 0.80 1.14 0.95 0.4 0.87 18 S018G 1.37 0.80 0.96 1.04 1.0 0.85 18 S018H 1.72 0.83 1.07 1.05 1.0 0.93 18 S018I 1.89 0.66 1.33 0.90 0.6 0.88 18 S018K 1.75 0.63 1.14 0.94 0.1 0.99 18 S018L 1.48 0.73 1.25 0.96 0.7 0.96 18 S018M 1.72 0.93 1.28 1.04 0.9 0.91 18 S018N 1.68 0.59 1.12 0.94 1.1 0.91 18 S018P 1.19 0.65 1.06 0.83 1.3 0.75 18 S018Q 1.68 0.80 1.12 0.99 1.0 0.92 18 S018R 1.61 0.71 0.99 1.02

0.93 18 S018T 1.64 0.67 1.25 0.99 1.1 0.89 18 S018V 1.67 0.57 1.17 1.14 0.8 0.89 18 S018W 1.59 0.73 1.06 1.00 0.4 0.95 18 S018Y 1.86 0.81 1.25 1.08 0.8 1.13 19 Q019A 1.82 1.07 0.99 1.05 0.8 0.92 19 Q019C 0.88 1.08 0.90 0.81 1.0 0.91 19 Q019D 0.87 0.98 0.95 0.67 1.1 0.98 19 Q019E 1.02 0.97 0.61 0.90 1.2 0.95 19 Q019F

19 Q019G 1.33 0.99 1.15 0.87 0.8 1.13 19 Q019H 0.82 1.05 0.98 0.72 0.9 1.08 19 Q019I 0.89 1.06 0.87 1.03 0.9 1.22 19 Q019K 0.86 0.87 0.78 0.77 0.6 1.15 19 Q019L 0.98 0.95 0.61 0.87 1.0 1.01 19 Q019M 0.90 1.02 1.01 0.90 0.7 0.96 19 Q019N

19 Q019P 0.38

0.08

19 Q019R 1.09 1.03 0.64 0.74 0.4 0.99 19 Q019S 0.82 1.03 1.14 0.92 0.8 1.07 19 Q019T 0.93 0.94 1.00 0.84 0.8 1.15 19 Q019V 0.88 1.12 1.04 0.97 0.7 1.22 19 Q019W

19 Q019Y

20 G020A 1.12 0.90 0.99 0.93 0.8 0.80 20 G020C 0.96 0.81 1.12 0.99 1.0 0.95 20 G020D 1.00 0.82 1.19 1.02 1.1 0.99 20 G020E 1.27 0.91 1.04 1.01 1.0 1.01 20 G020F 0.88 0.64 1.15 1.06 1.0 0.84 20 G020H 1.00 0.66 1.20 1.08 1.0 0.92 20 G020I 0.22 0.44 1.36 1.12 0.9 0.34 20 G020K 0.90 0.70 0.95 0.93 0.4 1.06 20 G020L 0.75 0.74 1.14 0.89 1.0 0.92 20 G020M 0.98 0.83 1.08 0.97 0.9 0.89 20 G020N 0.96 0.91 1.18 0.90 1.0 1.03 20 G020P 0.26 0.63 1.11 0.98 0.9 0.49 20 G020Q 0.95 0.53 1.13 1.01 0.9 1.06 20 G020R 0.86 0.70 0.99 0.92 0.2 0.99 20 G020S 1.00 0.63 1.07 1.05 0.7 0.88 20 G020T 0.54 0.82 1.24 1.08 0.9 1.02 20 G020V 0.22 0.97 1.37 1.53 0.8 0.40 20 G020W 0.63 0.88 1.15 1.05 0.8 0.93 20 G020Y 0.70 0.57 1.03 1.04 0.9 0.92 21 Y021A 1.15 0.85 0.77 0.94 0.9 0.81 21 Y021C 1.15 0.79 1.02 0.86 0.9 1.05 21 Y021D 0.84 0.83 0.76 1.02 0.9 0.73 21 Y021E 0.71 0.82 0.77 0.89 1.0 0.91 21 Y021F 1.13 0.59 0.77 0.97 1.0 0.85 21 Y021G 0.46 0.60 0.76 0.89 1.0 0.52 21 Y021H 1.22 0.78 0.69 0.98 1.1 0.93 21 Y021K 0.72 0.61 0.47 1.00 0.8 0.91 21 Y021L 0.92 0.78 0.75 0.99 1.0 0.95 21 Y021M 1.17 0.88 0.87 0.95 1.0 0.78 21 Y021P 0.47 0.50 0.88 1.08 1.2 0.69 21 Y021Q 0.74 0.88 0.87 1.02 0.9 0.96 21 Y021R 0.95 0.70 0.77 0.94 0.7 0.91 21 Y021S 0.98 0.71 0.84 0.93 0.9 0.80 21 Y021T 1.33 0.81 0.76 0.93 1.0 0.90 21 Y021V 1.15 0.70 0.99 1.00 1.1 0.87 21 Y021W 0.83 0.68 0.70 1.04 1.0 1.14 22 T022A 0.67 0.85 0.92 0.86 1.2 0.80 22 T022C 1.21 1.12 0.74 1.08 1.3 1.13 22 T022D 0.76 0.98 0.74 1.03 1.3 0.97 22 T022E 1.33 1.01 0.89 0.90 1.6 1.04 22 T022F 1.37 1.09 0.73 1.06 1.2 0.90 22 T022G 1.60 1.00 0.92 1.02 1.2 0.87 22 T022H 1.17 1.09 0.88 1.14 1.1 0.99 22 T022I 1.26 1.17 0.91 1.28 1.0 1.08 22 T022K 1.19 0.78 0.73 1.02 0.4 1.25 22 T022L 0.92 0.90 0.73 1.07 0.9 0.92 22 T022M 1.34 0.92 0.85 1.07 1.0 1.13 22 T022N 1.13 0.90 0.95 1.03 1.2 1.07 22 T022P 0.58 0.78 0.62 0.89 1.3 0.52 22 T022Q 1.42 1.15 0.75 1.14 1.1 0.97 22 T022S 1.10 0.95 0.91 0.98 1.3 0.93 22 T022V 1.32 1.18 0.75 1.10 1.3 1.11 22 T022W 1.52 0.93 0.79 1.07 1.7 0.87 22 T022Y 1.15 0.96 0.95 1.03 1.4 0.95 23 G023A 0.63 1.05 0.84 1.02 1.0 0.79 23 G023C 0.19 0.17

0.13

23 G023D 0.23

23 G023F 0.22 0.11 0.06

23 G023H 0.21 0.11

0.08

23 G023I 0.19

0.15

23 G023K 0.38

23 G023L 0.20 0.26 0.06 0.15

23 G023M 0.31

23 G023N 0.19

0.14

23 G023P 0.30 0.08

0.06

23 G023Q 0.26 0.08

0.10

23 G023R 0.22 0.14

23 G023S 0.17 10.83  4.09 2.61 1.1 0.13 23 G023T 0.21 0.16

23 G023V 0.14

0.26

23 G023W 0.25 0.10

23 G023Y 0.15

0.50

24 S024C 1.12 1.15 0.86 0.94 1.1 0.97 24 S024F 1.07 1.15 0.93 1.05 1.0 1.22 24 S024G 0.56 0.92 0.68 1.01 1.2 0.68 24 S024H 0.97 1.11 0.98 1.18 1.1 1.28 24 S024I 1.02 1.16 1.02 1.15 1.1 0.98 24 S024K 1.17 1.03 0.82 1.04 0.9 0.97 24 S024L 1.17 1.02 1.01 1.02 1.2 1.16 24 S024M 1.15 1.07 0.98 1.02 1.2 0.88 24 S024N 1.16 0.99 0.88 1.11 1.2 1.01 24 S024P 0.44 1.10 0.76 0.96 1.1 0.72 24 S024Q 0.90 0.96 0.94 1.11 1.0 1.10 24 S024R 0.86 1.19 0.82 1.12 1.0 1.19 24 S024T 0.57 1.07 0.92 1.06 1.1 0.96 24 S024V 0.45 1.21 0.93 1.19 1.1 1.22 24 S024W 1.13 1.09 0.62 1.09 1.2 0.94 24 S024Y 1.06 0.95 0.83 0.96 1.1 1.19 25 N025A 0.73 0.63 1.09 1.00 0.9 0.93 25 N025C 0.23

0.29 0.10 1.4 0.07 25 N025D

25 N025E 1.31 0.61 1.16 1.03 1.2 1.13 25 N025F 1.09 0.69 1.14 1.12 1.1 0.97 25 N025G 1.21 0.65 1.20 0.99 1.0 1.05 25 N025H 1.16 0.57 1.06 1.07 1.1 0.98 25 N025I 0.95 0.72 1.29 0.83 1.0 1.00 25 N025K 0.96 0.64 1.04 0.96 1.0 0.99 25 N025L 0.64 0.62 1.02 1.09 1.1 0.98 25 N025M 1.31 0.82 1.18 1.04 1.0 1.01 25 N025P 0.71 0.53 1.10 0.81 0.8 0.82 25 N025Q 1.10 0.61 1.21 1.09 1.0 1.08 25 N025R 1.34 0.68 1.02 1.12 1.0 1.03 25 N025S 0.85 0.60 1.18 1.01 1.0 0.93 25 N025T 1.06 0.73 1.21 1.12 0.8 1.22 25 N025V 0.59 0.45 1.27 1.11 0.9 1.01 25 N025W 1.42 0.53 1.30 1.00 0.9 0.99 25 N025Y

26 V026C 1.14 0.96 0.91 1.02 1.0 0.88 26 V026D 0.16

31.85 1.1 0.33 26 V026E 0.36 1.12 0.79 1.19 1.0 0.87 26 V026F 0.35 0.97 0.90 1.19 1.1 0.68 26 V026G 0.54 0.91 0.75 1.07 1.0 0.82 26 V026H 0.46 1.45 0.86 1.19 1.1 0.89 26 V026I 0.91 0.75 0.70 1.09 1.2 0.90 26 V026K 0.77 1.03 0.67 1.11 1.1 0.95 26 V026L 0.59 0.92 0.85 0.96 1.0 1.03 26 V026M 0.80 0.90 0.85 0.98 1.0 0.90 26 V026N 0.44 1.00 0.79 1.21 1.0 0.96 26 V026P 0.14

0.8 0.16 26 V026Q 0.61 0.96 0.78 1.02 1.0 1.08 26 V026S 0.82 0.82 0.85 0.95 0.9 0.86 26 V026T 0.92 0.98 0.98 1.02 0.9 1.04 26 V026W 0.25 2.33 1.16 2.13 1.1 0.95 26 V026Y 0.31 1.34 1.28 1.50 1.0 0.98 27 K027A 1.08 0.76 1.13 1.05 1.0 1.07 27 K027C

27 K027D 1.15 0.72 1.10 1.00 1.1 0.93 27 K027E 0.45 0.93 1.11 1.09 1.0 1.06 27 K027F 0.25 0.76 1.59 1.33 1.1 0.58 27 K027G 0.76 0.65 1.27 0.95 1.0 1.15 27 K027H 1.03 0.72 1.19 0.99 1.1 1.10 27 K027I 0.18 0.49 1.78 0.91 1.4 0.20 27 K027L 0.76 0.72 1.29 0.87 1.1 0.89 27 K027M 0.64 0.71 1.31 0.91 1.0 1.06 27 K027N 0.17

2.56 0.87 0.9 0.09 27 K027P 0.18 1.31 3.37 2.05 1.1 0.46 27 K027Q 0.15 0.58

1.5 0.08 27 K027R 1.09 0.64 1.16 0.96 1.0 1.19 27 K027S 0.93 0.92 1.11 1.04 1.0 1.11 27 K027T 0.56 0.85 1.39 1.09 1.0 1.09 27 K027V 0.23

0.18 0.06

27 K027W 0.36 0.69 1.47 1.33 0.9 0.93 27 K027Y 0.45 1.00 1.19 1.03 0.9 0.96 28 V028A 0.46 0.95 0.84 1.02 0.9 0.72 28 V028C 0.65 1.20 0.99 1.08 1.0 0.94 28 V028D 0.58

28 V028E 0.16

3.97 1.0 0.17 28 V028G 0.16

2.42

28 V028H 0.20 1.08 0.79 1.03 1.1 0.22 28 V028I 1.02 1.27 1.00 1.06 1.1 0.87 28 V028M 1.05 0.99 0.68 0.91 0.6 0.70 28 V028N 0.21 0.31 0.67 0.50 1.1 0.13 28 V028P 0.53 0.06

28 V028Q 0.18 2.79 1.99 1.43 1.6 0.25 28 V028R 0.40

28 V028S 0.18 5.70 5.17 3.40 1.1 0.37 28 V028T 0.58 1.31 1.18 1.13 1.0 1.21 28 V028W 0.31 0.07

28 V028Y 0.20 0.68 0.48 0.81

0.08 29 A029C 0.76 1.32 1.19 1.13 0.9 0.77 29 A029D 0.19 2.95 2.74 2.34 0.9 0.42 29 A029E 0.23 0.06

0.09

29 A029F 0.42

29 A029G 0.94 1.08 0.88 1.06 1.0 1.11 29 A029H 0.47

29 A029K 0.47 0.06

29 A029L 0.24 0.35 0.12 0.26

29 A029N 0.32 0.09

0.07

29 A029P 0.52

29 A029Q 0.33 0.12

29 A029R 0.42

29 A029S 0.47 1.64 1.13 1.23 1.1 1.01 29 A029T 0.24 2.02 1.55 1.57 1.1 0.47 29 A029V 0.38 1.85 1.52 1.62 1.0 0.83 29 A029W 0.34

29 A029Y 0.41

30 V030A 0.38 0.98 1.04 0.87 0.9 0.41 30 V030C 0.91 0.83 0.85 0.99 1.0 0.37 30 V030D 0.20 2.34 2.31 1.96 0.9 0.22 30 V030E 0.17 30.23  33.27  4.25 0.8 0.15 30 V030F 0.33 1.08 1.27 1.17

30 V030G 0.17 7.55 3.71 1.39

30 V030H 0.26 0.57 0.61 0.60

30 V030I 1.15 1.16 1.03 1.07 1.1 0.82 30 V030L 1.24 1.09 0.86 0.87 1.0 0.24 30 V030M 0.89 0.66 0.80 0.79 0.8 0.11 30 V030N 0.25 1.06 1.30 1.50 1.1 0.15 30 V030P 0.27 0.13 0.13 0.09

30 V030Q 0.21 0.82 0.99 1.10

30 V030R 0.20 0.13

0.22

30 V030S 0.28 1.25 1.21 1.43 0.3 0.12 30 V030T 0.30 1.39 1.27 1.38 0.9 0.37 30 V030W 0.26 0.11

0.08

30 V030Y 0.21 0.43

0.21

31 I031A 0.90 0.96 0.85 0.97 1.1 1.64 31 I031C 0.94 1.16 0.87 1.02 1.1 1.53 31 I031D 0.20 1.18 1.43 1.13 1.2 0.28 31 I031E 0.21 2.56 1.98 2.40 1.1 1.12 31 I031F 0.92 1.26 0.92 1.00 1.1 1.89 31 I031G 0.17 5.42 3.74 2.40 1.1 0.40 31 I031H 0.26 1.98 1.57 1.79 1.3 1.22 31 I031K 0.32 1.84 1.28 1.39 1.2 1.03 31 I031L 1.12 0.89 0.88 0.85 1.2 1.70 31 I031M 1.21 0.98 0.83 0.99 1.1 1.60 31 I031N 0.23 2.34 2.01 1.96 1.3 0.74 31 I031P 0.24 0.16 0.06 0.17 1.5 0.09 31 I031Q 0.19 5.38 3.51 3.08 1.1 0.64 31 I031R 0.31 0.10

31 I031S 0.21 3.71 2.83 2.91 1.1 0.86 31 I031T 0.38 1.21 1.04 0.91 1.1 1.17 31 I031V 0.83 1.03 1.09 1.03 0.9 1.20 31 I031W 0.29 0.13

31 I031Y 0.21 4.14 3.02 3.08 0.9 0.90 32 D032A 0.36

0.13

32 D032C 0.46 0.23 0.09 0.14

32 D032E 0.36 0.24

0.12

32 D032G 0.56

32 D032I 0.26 0.14

0.06

32 D032K 0.27 0.15

32 D032L 0.28 0.06

32 D032M 0.30 0.12

0.06

32 D032N 0.29 0.12

32 D032P 0.28 0.12 0.10 0.08

32 D032Q 0.27 0.16 0.14 0.10

32 D032R 0.27 0.17

32 D032S 0.40

32 D032T 0.27

32 D032V 0.30 0.20

32 D032Y 0.28 0.13 0.11

33 S033A 0.82 0.84 0.84 0.83 0.7 0.29 33 S033C 0.73 0.66 0.55 0.71 1.0 0.19 33 S033E 0.44 1.21 0.81 0.92 0.8 0.07 33 S033F 0.53 1.38 0.59 0.95

33 S033G 0.96 1.14 0.80 1.01 0.9 0.17 33 S033H 0.48 1.65 0.82 1.17

33 S033K 0.25 1.24 0.81 0.77

33 S033L 0.25 1.02 0.56 0.39

33 S033N 0.45 1.14 0.90 1.03 0.6 0.38 33 S033P 0.27 0.18

33 S033Q 0.36 0.69 0.72 0.72 0.5 0.13 33 S033R 0.33 1.10 0.53 0.80

33 S033T 0.82 0.74 0.64 0.85 1.0 1.40 33 S033V 0.50 0.56 0.57 0.54 0.9 0.09 33 S033W 0.34 1.15 0.39 0.51

34 G034A 0.27 0.81 0.91 0.81 0.5 0.09 34 G034C 0.26

0.12

34 G034D 0.28

0.06

34 G034E 0.27

0.06 0.13

34 G034F 0.29

0.12

34 G034H 0.32

0.07

34 G034I 0.26

0.07 0.10

34 G034K 0.29

34 G034L 0.30

34 G034M 0.30

0.12

34 G034N

34 G034P 0.45

34 G034Q 0.28

0.08 0.06

34 G034R 0.27

34 G034S 0.17

1.23 0.73

34 G034T 0.25

34 G034V 0.20

0.16 0.21

34 G034W 0.18 1.21 2.19 1.78

34 G034Y 0.21

0.13 0.11

35 I035A 0.59 0.82 1.14 0.92 0.9 0.69 35 I035C 0.95 0.65 1.41 1.06 1.0 0.95 35 I035D 0.29

0.08

35 I035E 0.24

0.12

35 I035F 0.17

1.52 0.33

35 I035G 0.18 0.21 1.85 1.07 1.0 0.16 35 I035H 0.26

35 I035K 0.16

2.01

35 I035L 0.61 0.68 1.14 1.03 0.7 0.74 35 I035M 0.33 0.71 1.27 1.07 0.8 0.59 35 I035N 0.20

0.34 0.09

35 I035P 0.38

35 I035Q 0.16

1.69 1.0 0.14 35 I035R 0.31

0.06

35 I035S 0.24 1.04 2.03 1.68 0.7 0.96 35 I035T 0.42 0.89 1.31 1.15 0.8 1.40 35 I035V 0.83 0.85 1.17 1.03 0.9 1.13 35 I035W 0.17

0.61

35 I035Y 0.16

10.64 

36 D036A 1.00 0.58 0.60 0.94 0.4 0.78 36 D036C 0.98 0.91 0.75 0.87 0.3 0.71 36 D036E 1.30 1.13 0.83 0.94 0.6 0.91 36 D036F 0.47 0.58 0.72 1.03

0.70 36 D036G 0.37 0.79 0.58 0.76

0.71 36 D036H 0.56 0.49 0.52 1.00 0.6 0.95 36 D036I 0.27 1.27 1.02 1.41

0.46 36 D036K 0.18

0.1 0.29 36 D036L 0.25 1.87 1.26 1.40

0.65 36 D036M 0.56 0.61 0.47 0.76

0.70 36 D036N 0.84 0.52 0.58 0.91

0.85 36 D036P 0.19

0.1 0.07 36 D036Q 0.67 0.62 0.54 0.99 0.9 0.98 36 D036R 0.17

0.14

0.14 36 D036S 1.03 0.72 0.70 0.87 0.1 0.93 36 D036T 0.72 0.64 0.45 0.87 0.1 0.85 36 D036V 0.54 0.92 0.69 0.88

0.83 36 D036W 0.71 0.80 0.70 0.82

0.85 37 S037A 1.25 1.14 1.07 0.73 0.9 1.03 37 S037C 1.09 0.90 0.87 0.93 1.0 0.94 37 S037D

37 S037E 0.72 0.83 1.06 0.84 1.0 0.92 37 S037F 0.99 1.05 0.88 0.91 1.0 0.83 37 S037G 1.21 1.19 0.95 0.95 1.0 1.25 37 S037H 1.04 1.06 0.98 0.90 0.9 1.04 37 S037I

37 S037K 1.31 0.98 0.63 0.84 1.1 1.02 37 S037L 0.98 1.04 0.91 0.78 0.8 0.87 37 S037M 1.31 1.00 1.07 0.82 0.9 0.87 37 S037N

37 S037P 0.48 1.48 0.90 1.13 0.4 0.70 37 S037Q 1.31 1.09 1.24 0.87 0.9 1.05 37 S037R 1.26 0.98 0.63 0.85 1.2 1.05 37 S037T 0.94 1.05 1.00 0.87 0.7 0.95 37 S037V 0.98 1.09 0.86 0.76 0.7 1.39 37 S037W 1.07 1.01 1.01 0.88 0.8 0.86 37 S037Y 0.19 0.21 0.16 0.13

38 S038A 1.17 1.14 1.06 1.03 0.9 0.90 38 S038C 1.27 0.96 1.02 1.03 1.2 0.82 38 S038D 0.67 1.26 1.19 1.07 1.2 0.97 38 S038E 1.31 1.02 1.11 0.97 1.3 0.84 38 S038F 0.97 0.99 0.97 1.07 1.0 1.22 38 S038G 1.43 1.01 1.04 1.13 0.9 0.97 38 S038H

38 S038I 1.07 0.98 1.08 1.01 1.1 0.89 38 S038K 1.25 0.75 0.80 1.02 1.3 0.93 38 S038L 1.06 0.90 1.11 1.12 1.1 1.02 38 S038M 1.33 1.10 1.07 1.00 1.0 0.91 38 S038N

38 S038P 1.16 1.12 0.93 0.99 0.5 0.76 38 S038Q 1.11 1.06 0.87 1.08 1.1 0.96 38 S038R 2.01 0.65 0.89 1.01 1.4 0.89 38 S038T 1.20 0.86 1.07 1.05 1.1 0.93 38 S038V 1.28 1.05 1.07 1.02 1.1 1.02 38 S038W 1.15 0.75 0.77 1.04 1.3 0.91 38 S038Y

39 H039A 0.29 0.81 1.17 1.04

0.76 39 H039C 0.96 0.80 1.08 0.99

1.00 39 H039D 0.20

0.11

39 H039E 0.18

0.22 0.09

39 H039F 0.26 0.70 1.65 1.18

0.73 39 H039G 0.15

0.1 0.10 39 H039I 0.50 1.02 1.03 0.97

1.18 39 H039K 0.33

39 H039L 0.27 0.87 1.31 1.42

0.84 39 H039M 0.24 0.98 1.54 1.16

0.64 39 H039N 0.77 0.82 1.02 1.32

0.92 39 H039P 0.23 0.12 0.09

39 H039Q 1.07 0.90 0.95 0.93 0.4 1.19 39 H039R 0.32

39 H039S 0.48 0.80 0.90 1.02

0.96 39 H039T 0.37 1.07 1.35 1.31

1.20 39 H039V 0.69 0.85 1.10 1.17

1.13 39 H039W 0.87 0.88 1.00 1.04

1.10 39 H039Y 0.14 0.50

40 P040A 1.01 1.23 1.09 1.08 0.8 1.22 40 P040C 0.99 1.04 1.19 1.15 1.1 1.12 40 P040D

40 P040E 1.21 1.05 1.34 1.05 1.6 1.01 40 P040F 0.92 1.12 1.21 1.09 0.9 1.02 40 P040G 1.06 1.04 1.11 1.14 0.1 1.11 40 P040H 0.89 0.97 0.98 1.17 0.5 1.09 40 P040I 0.83 1.12 1.30 1.10 0.7 1.23 40 P040K 1.20 0.78 0.96 0.99

1.02 40 P040L 1.06 1.20 1.05 1.10 1.0 1.09 40 P040M 1.01 1.07 1.24 1.10 0.6 0.98 40 P040N 0.88 1.12 1.14 1.07 0.5 1.18 40 P040Q 1.01 1.16 1.13 1.11 1.1 1.01 40 P040R 1.10 0.76 0.84 1.11

1.03 40 P040S 0.84 1.15 1.06 0.81 0.3 1.12 40 P040T 0.81 1.29 1.68 1.22 0.1 1.20 40 P040V 0.91 1.04 1.07 1.09 0.7 1.06 40 P040W 1.09 0.87 0.90 1.13 1.0 1.12 40 P040Y 0.89 1.07 1.07 1.06 0.5 1.02 41 D041A 0.22 2.48

0.77 0.1 0.18 41 D041C 0.26 1.70 0.30 1.07

0.48 41 D041E 0.67 1.07 1.03 0.91

0.92 41 D041F 0.29 0.13

41 D041G 0.17

0.1 0.10 41 D041H

41 D041I

41 D041K 0.23 1.13 0.27 0.22

41 D041L 0.26 0.10

0.09

41 D041M 0.21 10.40 

0.63

41 D041N 0.25 2.10 1.29 1.42

0.45 41 D041P 0.40

41 D041Q 0.19

13.41

0.15 41 D041R 0.41

41 D041S 0.23 3.12 1.52 1.20 0.5 0.33 41 D041T 0.19

0.19

41 D041V 0.18

41 D041W 0.14

41 D041Y 0.19

11.39

42 L042A 0.18

0.58 0.48 0.4 0.13 42 L042C 0.41 0.71 0.95 1.06 0.2 1.08 42 L042D 0.29

42 L042E

42 L042F 0.32 0.81 0.79 0.99

0.57 42 L042G 0.16

12.92 

42 L042H 0.23 0.98 1.26 1.11 0.3 0.38 42 L042I 1.15 0.87 0.56 0.92 0.8 0.77 42 L042K

42 L042M 0.80 1.20 0.99 1.00 0.7 0.92 42 L042N 0.23 0.80 0.86 1.21 0.6 0.48 42 L042P 0.38

42 L042Q 0.14

0.2 0.07 42 L042R 0.33

42 L042S 0.16 32.78 

0.37

42 L042T

42 L042V 0.97 0.96 0.88 0.98 0.5 0.82 42 L042W 0.14 0.18

42 L042Y 0.17 3.62 4.35 1.94

0.35 43 K043A 0.87 0.67 1.08 0.90 1.2 1.01 43 K043C 0.83 0.60 1.17 0.89 1.4 0.99 43 K043D 0.88 0.70 1.16 0.71 1.3 1.03 43 K043E 0.80 0.56 1.04 0.74 1.3 1.13 43 K043F 0.74 0.72 1.24 0.78 1.3 1.02 43 K043G 0.96 0.88 0.82 0.93 1.3 1.06 43 K043H

43 K043I 0.72 0.57 1.12 0.95 0.7 1.17 43 K043L 0.96 0.58 0.88 0.84 1.3 0.88 43 K043M 1.02 0.79 1.19 0.97 1.1 1.07 43 K043N 0.80 0.85 1.31 0.81 1.2 1.32 43 K043P 0.77 0.67 1.11 0.88

1.02 43 K043Q 0.95 0.61 1.09 0.90 1.3 1.05 43 K043R 1.14 0.56 1.30 0.87 0.9 1.33 43 K043S 0.98 0.77 1.14 0.92 1.3 0.99 43 K043T 0.93 0.92 1.06 0.96 1.1 1.07 43 K043V 1.10 0.59 0.98 0.93 0.6 1.26 43 K043W 0.85 0.67 0.98 0.90 1.3 1.03 43 K043Y 0.87 0.67 1.12 0.82 1.1 1.60 44 V044A 0.71 0.91 1.16 1.01 0.7 0.81 44 V044C 0.93 0.94 1.26 0.79 0.8 0.90 44 V044D

44 V044E 0.18 0.71 2.18 1.98 0.5 0.19 44 V044F 0.22 0.77 2.45 1.34

44 V044G 0.21 0.75 1.66 1.12 0.5 0.34 44 V044H 0.19 1.63 2.57 1.57 0.5 0.38 44 V044I 0.92 0.76 0.98 1.07 0.9 1.08 44 V044K 0.22

0.70 0.36 0.6 0.13 44 V044L 0.85 0.67 1.03 0.85 0.8 0.88 44 V044M 0.65 0.95 1.33 1.03 0.6 0.82 44 V044N 0.16

1.41 0.5 0.13 44 V044P 0.67 0.83 1.25 1.03 0.4 0.78 44 V044Q 0.20 1.48 2.85 1.49 0.6 0.33 44 V044R 0.19 0.79 1.62 0.69 0.2 0.13 44 V044S 0.33 1.03 1.51 1.13 0.5 0.86 44 V044T 0.30 1.32 1.94 1.30 0.7 1.26 44 V044W 0.13

0.4 0.06 44 V044Y 0.62 0.79 1.22 1.13 0.7 1.04 45 A045C 1.09 0.89 0.76 0.89 1.2 1.05 45 A045E 1.06 1.10 0.97 0.82 1.2 1.07 45 A045F 1.04 0.88 0.81 1.00 1.0 1.11 45 A045H 1.04 0.86 0.76 0.91 1.1 1.11 45 A045I 1.07 1.08 0.81 1.16 1.2 1.03 45 A045K 1.05 1.00 0.69 1.06 0.9 1.03 45 A045L 1.03 0.72 0.82 0.99 1.0 1.19 45 A045M 1.15 1.02 0.87 1.00 1.2 1.09 45 A045N 1.35 1.03 0.91 0.88 1.1 1.03 45 A045P 0.87 0.82 0.90 0.96 0.7 1.20 45 A045Q 1.07 0.84 0.95 1.09 1.1 1.16 45 A045R 0.18

1.0 0.11 45 A045S 1.08 0.93 0.87 0.86 1.2 1.02 45 A045T 0.99 1.04 1.31 0.90 1.2 1.01 45 A045V 1.28 0.85 0.81 1.03 1.1 1.12 45 A045Y 1.03 0.81 0.67 0.73 1.1 1.13 46 G046A 0.92 1.09 0.97 1.00 1.0 0.90 46 G046C 0.39 1.28 0.81 0.90 1.1 0.82 46 G046E 0.57 1.10 0.70 0.95 1.0 1.16 46 G046F 0.39 1.40 0.95 1.03 1.0 0.88 46 G046H 0.48 0.98 0.99 1.25 1.0 1.20 46 G046I 0.20

5.77 0.9 0.43 46 G046K 0.44 0.88 0.72 1.09 0.8 1.20 46 G046L 0.27 1.57 1.44 1.42 0.8 0.78 46 G046M 0.42 1.30 0.84 1.14 0.9 0.96 46 G046N 0.69 0.79 0.72 1.05 1.1 0.94 46 G046P 0.17

0.9 0.06 46 G046Q 0.15

1.5 0.23 46 G046S 0.74 0.86 0.78 0.94 0.9 1.16 46 G046T 0.39 1.21 0.96 0.79 0.8 1.04 46 G046V 0.23 4.92 3.26 2.09 0.8 0.74 46 G046W 0.44 1.08 0.66 0.90 1.0 1.13 46 G046Y 0.36 1.02 1.27 1.12 0.8 1.23 47 G047A 0.32 0.98 0.96 1.04 0.5 0.30 47 G047C 0.24 0.64 1.09 0.88 0.6 0.15 47 G047D

47 G047E 0.23 0.72 0.99 1.02 0.6 0.14 47 G047F 0.25 0.96 0.86 1.15 0.5 0.15 47 G047H 0.23 1.04 1.17 1.20 1.1 0.47 47 G047I 0.17 1.25 1.59 1.31

47 G047K 0.16

2.16

47 G047L 0.17

2.78 0.82

47 G047M 0.22 0.63 0.89 0.87 0.5 0.10 47 G047N 0.16

2.54 0.5 0.06 47 G047P 0.39

47 G047Q 0.16

6.49 0.6 0.14 47 G047R 0.16

7.73 1.41

47 G047S 0.21 1.19 1.04 1.24 0.5 0.15 47 G047T 0.17 4.45 4.77 2.27 0.5 0.12 47 G047V 0.16

5.71 0.6 0.13 47 G047W 0.18 2.60 2.43 2.22 0.5 0.17 47 G047Y

48 A048C 1.15 1.14 1.16 0.85 1.1 0.95 48 A048D 1.13 1.01 1.00 0.97 1.1 0.89 48 A048E 1.17 0.84 0.93 1.02 1.2 0.90 48 A048F 1.08 1.08 0.92 0.96 1.0 0.89 48 A048H 1.08 0.87 1.16 1.04 1.1 0.87 48 A048I 1.02 0.79 0.91 1.02 1.2 1.00 48 A048K 1.13 0.90 0.55 0.91 1.1 0.90 48 A048L 0.99 0.87 0.97 0.99 1.0 0.91 48 A048M 0.59 1.21 0.99 0.87 1.1 0.92 48 A048P 0.17

1.0 0.22 48 A048Q 1.10 0.83 0.69 1.03 1.0 1.02 48 A048R 1.11 0.83 0.51 0.98 0.9 1.05 48 A048S 0.98 1.08 0.47 1.06 1.0 1.03 48 A048T 0.98 1.06 0.77 0.84 1.1 0.97 48 A048V 1.47 0.99 0.61 0.92 1.0 0.94 48 A048W 0.81 0.69 0.74 0.81 0.9 1.04 48 A048Y 1.03 0.84 0.81 0.86 1.0 0.90 49 S049A 0.35 0.54 0.61 1.02 0.9 0.30 49 S049C 0.61 0.48 0.69 0.97 0.5 0.38 49 S049D 0.23 1.09 1.53 1.69 0.5 0.36 49 S049E 0.27

49 S049F 0.33

49 S049G 0.28 0.78 0.75 1.64 1.2 0.50 49 S049H 0.23 0.12 0.39 0.39

49 S049I 0.18 2.22 2.52 2.14 0.5 0.11 49 S049K 0.23

0.17

49 S049L 0.23

0.10

49 S049N 0.35 1.04 0.88 1.32 0.5 0.64 49 S049P 0.30

0.09

49 S049Q 0.23

0.07 0.18

49 S049R 0.33

49 S049T 0.29 0.95 1.23 1.37 0.5 0.46 49 S049V 0.21 1.58 1.39 2.10 0.4 0.30 49 S049W 0.20

49 S049Y 0.27

50 M050A 0.78 1.16 0.85 0.89 0.9 1.09 50 M050C 0.89 1.17 0.89 0.80 1.1 1.01 50 M050D 0.17 6.35 0.87 0.90 1.0 0.16 50 M050F 0.95 1.01 0.96 0.81 1.1 1.09 50 M050H 0.85 1.22 0.98 0.95 1.2 1.01 50 M050I 0.33 1.61 0.91 1.09 0.9 0.55 50 M050K 0.49 0.80 0.67 0.79 1.1 1.07 50 M050L 0.91 0.76 1.02 0.96 1.1 1.00 50 M050N 0.35 1.03 0.86 1.07 1.0 1.11 50 M050P 0.20 0.64

0.16

50 M050Q 0.76 1.23 0.93 1.03 1.1 1.01 50 M050R 0.25 1.38 0.73 1.07 1.0 0.82 50 M050S 0.81 1.08 0.89 1.05 1.0 1.08 50 M050T 0.87 1.05 0.90 1.04 1.1 1.38 50 M050V 0.70 1.08 0.82 1.02 1.1 0.82 50 M050W 1.06 1.10 0.80 0.78 1.0 1.16 50 M050Y 0.70 1.03 0.87 0.89 1.0 1.19 51 V051A 0.38 1.41 1.25 1.22 0.9 0.43 51 V051C 0.91 1.02 1.16 1.02 1.1 0.41 51 V051D 0.34 1.02 1.32 1.12 1.0 0.50 51 V051E 0.39 1.17 1.59 1.26 1.0 0.59 51 V051F

51 V051G 0.22 3.43 4.27 1.35

51 V051H 0.86 0.59 1.06 0.98 1.2 0.79 51 V051I 0.69 0.79 1.23 1.12 1.1 0.95 51 V051K

51 V051L 0.48 0.73 1.21 0.87 1.0 0.59 51 V051M 0.60 0.97 1.07 1.10 1.0 0.67 51 V051N

51 V051P 0.20

4.63

51 V051Q 0.28 1.26 1.81 1.14 0.9 0.40 51 V051R 0.18

1.3 0.10 51 V051S 0.32 1.84 1.95 1.43 0.9 0.35 51 V051T 0.46 0.98 1.16 1.03 0.9 0.75 51 V051W 0.18

51 V051Y 0.25 1.20 1.58 1.76 0.9 0.31 52 P052A 0.56 1.22 1.25 1.17 0.7 0.59 52 P052C 0.34 1.36 1.56 0.94 1.0 0.44 52 P052D 0.79 1.27 1.50 1.21 0.9 0.76 52 P052E 0.89 1.12 1.54 1.20 0.9 0.75 52 P052F 0.41 0.87 1.13 1.14 0.9 0.51 52 P052G 0.44 1.05 1.42 1.24 0.8 0.53 52 P052H 0.45 0.97 1.28 1.04 0.9 0.47 52 P052I 0.45 1.33 1.50 1.11 0.8 0.61 52 P052K 0.38 0.86 1.09 1.35 0.8 0.53 52 P052L 0.46 1.33 1.24 1.32 0.8 0.61 52 P052M 0.43 1.40 1.30 1.06 0.7 0.54 52 P052N

52 P052Q 0.43 0.83 1.48 1.20 0.8 0.63 52 P052R 0.33 1.02 1.31 1.26 0.7 0.58 52 P052S 0.51 1.02 1.55 1.26 0.8 0.60 52 P052T 0.47 1.23 1.73 1.09 0.8 0.61 52 P052V 0.31 1.79 1.63 1.03 1.0 0.50 52 P052W 0.36 1.49 1.34 1.43 1.0 0.77 52 P052Y 0.35 1.55 1.42 1.32 1.0 0.55 53 S053A 1.37 1.07 1.15 1.03 1.0 0.87 53 S053C

53 S053D

53 S053E 1.52 1.05 1.16 1.12 1.0 0.98 53 S053F 1.19 0.91 1.05 0.87 1.0 1.11 53 S053G 1.72 1.15 1.19 0.94 1.0 0.86 53 S053H 1.35 0.96 1.02 0.96 1.1 0.84 53 S053I 1.22 0.97 1.10 0.80 1.0 0.90 53 S053K 1.36 0.89 0.93 0.76 1.1 0.95 53 S053L 1.18 0.92 0.97 1.00 1.1 0.90 53 S053M 1.54 1.01 0.98 0.97 0.8 0.80 53 S053N 1.48 0.95 1.04 1.15 1.1 0.87 53 S053P 0.46 1.01 1.39 0.94 0.9 0.85 53 S053Q 0.76 0.85 1.30 1.09 1.1 1.05 53 S053R 1.06 0.68 0.82 0.87 1.1 1.00 53 S053T 1.33 1.05 1.23 0.85 1.0 0.94 53 S053V 1.13 1.11 1.20 1.10 1.1 0.95 53 S053W 1.49 0.86 1.02 0.80 0.9 0.98 53 S053Y

54 E054A 0.89 0.97 1.07 0.83 0.6 0.66 54 E054C 0.71 0.94 1.05 0.85 0.8 0.68 54 E054D

54 E054F 0.51 0.86 0.97 0.93 0.7 0.63 54 E054G 0.38 1.27 0.59 1.04 0.5 0.42 54 E054H 0.73 0.69 0.80 0.96 0.8 0.67 54 E054I

54 E054K 0.35 1.03 1.14 1.07 0.8 0.60 54 E054L 0.49 1.00 1.02 0.87 0.8 0.71 54 E054M 0.63 1.06 0.99 1.03 0.7 0.61 54 E054N 0.97 0.99 1.03 1.06 0.8 0.76 54 E054P 0.19 0.47 1.13 1.34 0.6 0.17 54 E054Q 0.97 1.00 0.99 1.04 0.8 0.90 54 E054R 0.24 1.47 1.83 1.68 0.6 0.55 54 E054S 0.98 0.97 0.97 0.96 0.8 0.69 54 E054T 0.52 1.02 1.11 0.93 0.6 0.70 54 E054V 0.41 1.12 1.34 1.11 0.6 0.78 54 E054W 0.31 1.18 1.18 1.01 0.6 0.71 54 E054Y 0.42 1.03 0.99 1.00 0.8 0.69 55 T055A 1.11 0.63 0.98 1.00 1.0 0.96 55 T055C 1.41 0.64 1.06 0.89 1.1 0.86 55 T055D 0.76 1.01 1.26 0.94 1.1 1.06 55 T055E

55 T055F 0.67 0.62 0.78 0.84 0.9 0.92 55 T055G 1.21 1.00 0.90 0.97 1.1 0.85 55 T055H 1.06 1.14 0.98 0.96 1.1 1.04 55 T055I 0.96 1.08 0.97 0.89 1.0 1.02 55 T055K 1.27 0.59 0.87 0.98 1.0 1.09 55 T055L 1.39 0.80 1.30 0.96 1.1 0.95 55 T055M 0.92 0.85 1.19 0.99 1.0 1.09 55 T055N

55 T055P 0.94 0.90 1.20 0.86 1.0 1.23 55 T055Q 1.06 0.87 1.20 0.91 1.1 1.06 55 T055R 1.14 0.54 0.81 0.90 1.0 1.01 55 T055S 1.00 1.03 1.32 0.94 1.1 0.99 55 T055V 0.98 0.54 1.20 0.97 1.0 1.10 55 T055W 1.06 0.68 0.81 0.92 1.0 0.95 55 T055Y 0.97 0.90 0.97 0.91 1.0 0.91 56 N056A 0.31 1.18 1.27 1.14 0.4 0.34 56 N056C

56 N056D 1.09 0.79 0.89 0.84 1.2 0.99 56 N056E 0.67 0.91 0.98 0.91 0.7 0.69 56 N056F 0.27 1.02 1.00 1.31 0.6 0.31 56 N056G 0.29 1.61 1.06 1.22 0.4 0.46 56 N056H 0.39 1.08 1.07 0.95 0.8 0.81 56 N056I 0.24 1.69 1.26 1.41 0.6 0.47 56 N056K 0.21 2.07 1.45 1.86 0.5 0.38 56 N056L 0.23 1.26 1.81 1.66 0.7 0.34 56 N056M 0.26 1.50 1.24 1.23 0.5 0.36 56 N056P 0.26 0.95 1.32 0.94 0.8 0.62 56 N056Q 0.29 1.74 1.29 1.22 0.8 0.41 56 N056R 0.17 4.90 3.96 2.20 0.5 0.27 56 N056S 0.99 0.78 0.97 0.92 0.9 0.77 56 N056T 0.58 0.90 1.08 1.04 0.6 0.65 56 N056V 0.27 1.36 1.29 0.99 0.5 0.49 56 N056W 0.36 1.28 1.33 1.16 0.6 0.48 56 N056Y 0.25 1.30 1.25 1.30 0.7 0.41 57 P057A 0.61 0.95 1.08 1.03 0.5 0.66 57 P057C 0.50 1.04 1.18 0.95 0.8 0.65 57 P057D 0.52 1.11 1.42 1.14 0.9 0.87 57 P057E 0.38 1.23 1.53 1.23 0.8 0.87 57 P057F 0.59 0.93 0.98 0.92 0.3 0.75 57 P057G 0.42 1.29 1.19 1.12 0.3 0.69 57 P057H

57 P057I 0.25 2.20 2.00 1.60 0.4 0.29 57 P057K 0.24 1.51 1.84 1.09 0.3 0.34 57 P057L 0.24 2.59 2.00 1.46 0.4 0.28 57 P057M 0.36 1.08 1.11 0.97 0.4 0.40 57 P057N 0.35 1.17 1.67 1.11 0.7 0.73 57 P057Q 0.35 1.25 1.38 1.04 0.5 0.65 57 P057R 0.23 2.31 3.14 1.52 0.4 0.42 57 P057S 0.39 0.91 1.10 0.97 0.5 0.65 57 P057T 0.25 2.53 1.97 2.27 0.5 0.56 57 P057V 0.22 3.61 5.95 3.50 0.3 0.48 57 P057W 1.03 0.61 1.05 0.94 0.7 0.86 57 P057Y

58 F058A 0.55 1.18 1.32 1.15 0.6 0.61 58 F058C 0.95 1.08 1.21 0.93 1.1 0.92 58 F058D 0.52 1.18 1.32 0.97 1.0 0.93 58 F058E 0.87 0.87 1.20 1.09 0.9 1.05 58 F058G 0.91 1.21 1.26 1.00 1.1 0.76 58 F058H 0.98 0.96 1.34 0.89 0.9 0.99 58 F058I 0.64 0.88 1.07 0.94 0.8 1.00 58 F058K 0.44 1.15 1.36 1.09 0.6 0.63 58 F058L 0.89 0.99 1.16 0.89 0.9 0.86 58 F058M 1.01 1.08 1.24 0.91 0.8 0.82 58 F058N 0.86 1.18 1.25 0.87 0.9 0.91 58 F058P 0.23 0.71 1.00 0.89 0.6 0.22 58 F058Q 0.60 1.22 1.20 0.93 0.6 0.80 58 F058R 0.49 0.75 1.06 0.95 1.0 0.73 58 F058S 0.61 1.21 1.10 1.03 0.6 0.81 58 F058T 0.36 1.36 1.76 1.16 0.7 1.01 58 F058V 0.73 1.01 1.09 1.05 0.7 0.98 58 F058W

58 F058Y 1.16 1.19 0.90 1.00 0.9 1.09 59 Q059A 1.27 0.91 1.18 0.96 0.9 0.96 59 Q059C 0.89 1.08 1.26 1.06 1.2 0.92 59 Q059D 1.42 1.09 1.31 0.88 1.2 1.01 59 Q059E 1.42 1.11 1.15 0.85 1.3 0.94 59 Q059F 1.18 0.97 1.13 0.85 0.9 0.93 59 Q059G 0.92 1.06 1.05 1.00 0.7 0.75 59 Q059H 1.24 0.91 1.00 1.14 1.0 0.91 59 Q059I

59 Q059K 1.31 0.83 0.87 0.87 0.9 0.94 59 Q059L 1.21 1.10 1.12 1.04 1.1 1.01 59 Q059M 1.26 1.18 1.08 0.95 1.1 0.95 59 Q059N 1.15 1.12 1.16 1.01 1.0 0.98 59 Q059P 0.27 1.86 2.01 1.47 0.8 0.43 59 Q059R 0.82 0.78 0.71 0.81 1.0 0.95 59 Q059S 1.25 1.13 1.15 0.94 0.8 0.97 59 Q059T 1.37 1.10 1.04 1.02 0.9 0.90 59 Q059V 1.38 1.14 1.14 1.14 1.0 1.21 59 Q059W 0.24 1.36 1.62 1.16 1.0 0.46 59 Q059Y 1.12 1.08 1.21 1.08 0.9 0.86 60 D060A 0.43 1.01 1.21 0.99 0.2 0.68 60 D060C 0.49 0.81 0.94 0.89 0.5 0.56 60 D060E 0.32 0.89 1.23 0.94 0.5 0.45 60 D060F 0.25 0.35 1.00 0.71 0.1 0.34 60 D060G 1.09 0.80 0.93 0.89 0.4 0.91 60 D060H 0.31 0.66 1.29 0.95 0.2 0.50 60 D060I 0.33 0.50 1.15 0.83 0.1 0.61 60 D060K

60 D060L 0.27 0.54 1.07 0.88 0.1 0.41 60 D060M 0.27 0.87 1.26 1.16 0.2 0.43 60 D060N 0.32 0.77 1.19 1.11 0.2 0.55 60 D060P 0.85 0.64 0.83 0.73 0.1 0.59 60 D060Q 0.26 0.97 1.35 1.03 0.2 0.57 60 D060R 0.35 0.31 0.65 0.63 0.1 0.62 60 D060S 0.40 0.83 0.96 1.00 0.2 0.74 60 D060T 0.30 0.95 1.72 1.28 0.2 0.78 60 D060V 0.39 0.77 0.91 0.98 0.1 0.74 60 D060W 0.21 0.57 1.17 1.22 0.1 0.35 60 D060Y 0.28 0.58 0.93 0.73 0.2 0.47 61 N061A 1.66 1.22 1.11 1.09 1.0 0.95 61 N061C 1.41 0.95 0.96 0.90 1.1 1.11 61 N061D 1.25 1.19 1.21 0.85 1.2 1.14 61 N061E 1.53 1.21 1.08 1.08 1.2 1.08 61 N061F 1.50 1.00 0.90 0.80 1.0 0.89 61 N061G 1.45 1.01 1.06 1.01 1.0 0.80 61 N061H 1.46 1.15 1.00 0.93 1.2 0.89 61 N061I 1.32 1.25 1.00 0.71 1.2 1.10 61 N061K 1.20 0.89 1.00 0.76 0.9 1.11 61 N061L 1.34 0.96 1.00 0.88 1.1 1.07 61 N061M 1.28 0.98 1.01 1.04 1.0 1.06 61 N061P 1.42 1.47 1.04 0.78 1.0 1.40 61 N061Q 1.27 0.90 1.08 0.88 1.0 1.14 61 N061R 1.42 0.67 0.71 0.86 0.8 1.09 61 N061S 1.06 1.00 0.98 0.88 0.9 1.51 61 N061T 1.14 0.98 0.98 0.99 1.1 1.19 61 N061V 1.43 1.02 1.03 0.77 1.0 1.19 61 N061W 1.42 1.12 0.80 0.83 1.1 0.94 61 N061Y 1.31 1.04 0.97 0.98 1.2 0.90 62 N062A 1.20 0.77 0.76 0.88 1.1 1.18 62 N062C 1.57 1.18 1.16 0.82 0.3 0.63 62 N062D 1.48 1.40 1.18 0.91 1.1 0.67 62 N062E 1.42 1.19 1.19 0.92 1.1 0.59 62 N062F 2.06 0.75 1.07 0.87 1.1 0.37 62 N062G 1.41 1.03 0.83 0.84 1.3 0.78 62 N062H

62 N062I 0.95 0.81 0.87 0.69 1.3 0.74 62 N062K 1.23 1.05 0.97 1.02 0.9 0.48 62 N062L 1.79 0.87 0.80 1.07 1.4 0.63 62 N062M 1.76 1.30 1.12 1.07 1.1 0.58 62 N062P

62 N062Q 1.45 1.32 1.23 1.06 1.2 0.60 62 N062R 1.33 1.13 0.73 0.94 0.9 0.29 62 N062S 0.65 1.14 0.97 0.91 1.0 1.06 62 N062T 0.96 1.21 0.97 0.86 1.1 1.01 62 N062V 1.43 0.86 1.00 0.57 1.1 0.56 62 N062W 1.56 1.27 1.25 0.79 1.1 0.11 62 N062Y 1.70 0.92 0.79 1.09 1.2 0.37 63 S063A 1.12 0.94 1.12 0.98 1.1 0.88 63 S063C 1.56 1.31 0.97 0.69 1.3 0.77 63 S063D 1.42 0.90 0.86 0.84 1.4 0.81 63 S063E 1.50 1.13 1.03 0.93 1.3 1.00 63 S063F 1.26 0.91 0.73 0.88 1.0 0.77 63 S063G 1.46 0.67 0.79 0.83 0.9 1.21 63 S063H 1.41 0.92 0.95 0.80 1.0 0.90 63 S063I

63 S063K 1.62 1.03 0.75 0.89 0.3 0.82 63 S063L 1.46 1.22 0.86 1.02 1.0 0.92 63 S063M 1.48 1.02 0.86 1.17 0.9 1.04 63 S063N 1.42 0.97 1.00 0.97 1.2 0.85 63 S063P 0.84 0.62 0.71 0.71 0.6 0.67 63 S063Q 1.55 1.36 0.81 1.05 1.0 0.98 63 S063R 1.58 0.93 0.65 0.83 0.1 1.03 63 S063T 1.03 1.33 1.03 1.01 1.0 0.93 63 S063V 1.19 1.13 0.88 0.98 0.7 1.35 63 S063W 1.26 0.84 0.93 0.67 0.9 2.18 63 S063Y 1.38 1.02 0.72 0.93 0.8 0.90 64 H064C 0.48 0.06

64 H064D 0.34 0.11

64 H064F 0.57

64 H064I 0.56 0.09

64 H064K 0.38 0.07

64 H064L 0.54 0.08

64 H064M 0.45

64 H064Q 0.57

64 H064R 0.44

64 H064S 0.81

64 H064T 0.70

64 H064V 0.49

64 H064Y 0.49

65 G065A 0.28 0.26 0.55 0.99

65 G065D 0.51

65 G065F 0.56

65 G065H 0.37 0.09

65 G065I 0.56

65 G065K 0.49

65 G065L 0.59

65 G065M 0.49

65 G065N 0.57

65 G065P 0.51

65 G065Q 0.23 1.74 2.07 2.34 1.2 0.66 65 G065R 0.48

65 G065S 0.38 0.07

0.24

65 G065T 0.52

65 G065V 0.43

65 G065W 0.53

65 G065Y 0.52

66 T066A 0.22

0.12

66 T066C

66 T066D 0.26

66 T066E 0.31

66 T066F 0.37

66 T066G 0.27

66 T066H 0.26

66 T066I 0.21

0.06 0.11

66 T066K 0.31

66 T066L 0.21

0.08

66 T066M 0.22

0.06

66 T066N 0.18

0.25

66 T066P 0.30

66 T066Q 0.22

66 T066R 0.30

66 T066S 1.10 0.87 0.95 0.89 0.6 0.81 66 T066V 0.15 0.14

66 T066W 0.32

66 T066Y 0.28

67 H067A 1.37 0.43 0.24 0.50 0.5 0.34 67 H067C 1.36 0.46 0.24 0.52 0.3 0.29 67 H067D 0.29 0.11

67 H067F 1.13 0.64 0.50 0.81 0.1 0.33 67 H067I 1.55 0.51 0.20 0.47 0.2 0.42 67 H067K 0.54 0.17

0.24

67 H067L 1.31 0.37 0.14 0.47 0.3 0.16 67 H067M 1.34 0.56 0.31 0.66 0.6 0.42 67 H067N 1.12 0.76 0.31 0.65 0.1 0.62 67 H067P 1.01 0.43 0.18 0.50 0.8 0.51 67 H067R 1.33 0.22 0.06 0.30

67 H067S 1.26 0.55 0.28 0.55 0.1 0.39 67 H067T 1.23 0.57 0.36 0.69 0.1 0.52 67 H067W 0.24 0.76 0.08 0.51

0.95 68 V068A 1.00 1.79 1.11 1.30 1.0 0.06 68 V068C 1.05 1.11 1.10 1.07 0.8 0.70 68 V068D 0.26 0.49 0.55 0.55

68 V068E

68 V068F 0.46

68 V068G 0.52 1.83 1.33 1.36

68 V068H 0.78

68 V068I 1.19 1.15 0.96 0.82 1.2 0.32 68 V068K 0.34

0.06

68 V068L 0.62 1.22 0.81 0.95

68 V068M 1.17 1.31 0.92 1.16

68 V068N 0.77 0.45 0.48 0.55

68 V068P 0.28 0.06 0.19 0.10

68 V068Q 1.26 0.14 0.19 0.25

68 V068R 0.33

68 V068S 1.25 1.74 1.26 1.12

68 V068T 0.94 1.17 1.06 0.79 0.6 0.42 68 V068W 0.38

68 V068Y 0.44

69 A069C 0.36 1.66 0.92 1.19 0.7 0.45 69 A069D 0.25 2.04

69 A069E 0.34 1.08

69 A069F 0.18 13.66  1.33 0.48

69 A069G 0.88 0.73 0.95 1.04 0.9 1.02 69 A069H 0.17 39.03  2.24 0.72 0.7 0.08 69 A069I 0.16

0.95

69 A069K 0.20

0.06

69 A069L 0.15 0.89

0.25

69 A069M 0.19 7.17 0.69 0.55 0.5 0.06 69 A069N 0.21 2.48 0.06

69 A069P 0.32 1.77

69 A069Q 0.22 5.22 0.06

69 A069R 0.35 2.01

69 A069S 0.85 0.61 0.70 1.17 0.9 0.93 69 A069T 0.48 1.58 0.96 1.02 1.0 0.72 69 A069V 0.15 0.31

69 A069W 0.15

5.05 1.0 0.12 69 A069Y 0.16

0.08

70 G070A 0.62

70 G070C 0.41

70 G070D 0.42 0.09

70 G070F 0.39 0.13

70 G070H 0.40 0.07

70 G070I 0.34 0.07

70 G070K 0.36

70 G070L 0.41

70 G070M 0.44

70 G070N 0.35

70 G070P 0.34 0.08

70 G070R 0.32 0.14

70 G070S 0.43

70 G070T 0.33 0.07

70 G070V 0.43

70 G070W 0.31 0.08

71 T071A 0.44 1.17 1.02 1.07 0.1 0.59 71 T071C

71 T071D 0.21 41.12  34.56  1.45 0.2 0.06 71 T071E 0.25 2.16 1.92 1.03 0.1 0.33 71 T071F 0.20 0.24 0.40

71 T071G 0.23 3.34 1.64 1.85

0.36 71 T071H

71 T071I 0.80 0.74 1.19 1.08 0.5 1.07 71 T071K 0.21 37.02  45.54  2.17 0.1 0.17 71 T071L 0.24 0.24

71 T071M 0.28 1.33 1.18 1.13

0.39 71 T071N 0.19

0.1 0.10 71 T071P 0.18

0.1 0.15 71 T071Q 0.20

2.94 0.1 0.09 71 T071R 0.18

71 T071S 1.14 0.87 1.17 1.17 0.5 0.89 71 T071V 0.74 0.85 1.00 0.99 0.5 0.86 71 T071W 0.18

71 T071Y 0.20

0.15

72 V072A 0.84 0.95 1.00 0.94 0.8 0.89 72 V072C 0.71 1.13 1.02 1.10 0.8 0.88 72 V072D 0.19 2.54 1.66 1.93 0.7 0.19 72 V072E 0.50 1.14 1.08 1.13 0.8 0.62 72 V072F 0.71 0.96 1.06 0.96 0.7 0.74 72 V072G 0.35 1.52 1.06 1.36 0.8 0.65 72 V072H 0.35 1.05 1.01 1.17 0.8 0.57 72 V072I 1.16 1.12 1.03 0.97 1.0 0.79 72 V072K 0.19 2.81 2.06 2.76 1.7 0.30 72 V072L 1.00 1.16 1.07 0.97 0.9 0.67 72 V072P 0.21 0.33

0.08

72 V072Q 0.27 1.63 1.54 1.67 0.6 0.64 72 V072R 0.37

72 V072S 0.36 1.36 1.41 1.34 0.8 0.91 72 V072T 0.63 1.37 1.01 1.09 0.9 0.99 72 V072W 0.21 0.20

0.13

72 V072Y 0.15

0.8 0.28 73 A073C 0.85 1.03 1.08 1.03 0.9 0.93 73 A073E 0.47 1.62 1.22 1.13 0.2 0.78 73 A073F 0.23

0.17

73 A073G 0.96 0.85 1.01 1.14 0.8 1.00 73 A073H 0.14

0.2 0.23 73 A073I 0.17 22.54  15.70  6.07 0.1 0.30 73 A073K 0.18 3.45 2.48 2.56 0.1 0.27 73 A073L 0.15

0.4 0.14 73 A073M 0.24 1.71 1.42 1.48 0.3 0.43 73 A073N 0.71 1.15 1.05 1.13

0.76 73 A073Q 0.55 1.31 1.33 1.14 0.5 0.93 73 A073R 0.14

73 A073S 1.02 1.35 0.94 1.00 0.8 1.06 73 A073T 0.71 1.27 1.06 1.15 0.6 1.11 73 A073V 0.38 1.42 1.19 1.46 0.1 0.83 73 A073W 0.38 0.10

73 A073Y 0.21

74 A074C 0.73 0.65 1.02 0.96

0.98 74 A074D

74 A074E 0.25 4.31

74 A074F 0.31 2.60

74 A074G 1.04 0.89 0.85 1.06 0.2 1.00 74 A074H 0.30 3.15

74 A074I 0.33 2.09

74 A074K 0.35 1.19 0.07

74 A074L 0.29 2.24

74 A074M 0.23 5.33

74 A074N 0.23

0.10

74 A074P 0.33 1.26

74 A074Q 0.26 2.88 0.06

74 A074R 0.29 1.85

74 A074S 1.11 0.77 0.91 1.14

0.95 74 A074T 0.15

0.1 0.12 74 A074V 0.26 3.59 0.06

74 A074W 0.29 2.54

74 A074Y 0.31 2.83 0.09

75 L075A 1.07 1.41 0.96 1.03

1.01 75 L075C 1.10

1.09 0.99 0.2 1.09 75 L075D 0.76

0.77 1.09

1.06 75 L075E 1.09

0.87 1.10

1.12 75 L075F 0.55

1.00 0.96

0.93 75 L075G 0.90 0.63 0.86 1.02

1.12 75 L075H 0.75

0.82 0.95

1.04 75 L075I 0.97

0.70 1.08 0.1 1.08 75 L075K 0.93

0.61 0.95 0.1 1.12 75 L075M 1.03 0.67 0.71 1.06

0.97 75 L075N 0.82

0.61 0.91

0.96 75 L075P 0.38

0.82 1.09

0.87 75 L075Q 1.18

0.68 1.16 0.1 1.09 75 L075R 0.95

0.95 1.09 0.1 1.00 75 L075S 0.88 0.70 0.57 1.11

1.08 75 L075T 0.96

0.64 0.97

1.13 75 L075V 1.08

0.67 1.17 0.1 1.04 75 L075W 0.62

0.97 1.06

1.18 75 L075Y 0.48 1.23 0.83 0.97

0.95 76 N076A 1.05 1.69 0.75 0.99

1.03 76 N076C 0.86

0.64 0.86 0.2 1.06 76 N076D 1.26

0.74 0.89 1.9 1.04 76 N076E

76 N076F 0.95 0.51 0.61 1.03

0.94 76 N076G 0.97 1.00 0.63 1.00

1.21 76 N076H 1.29

0.70 1.03 0.3 1.01 76 N076I 1.08

0.80 0.96

0.95 76 N076K 0.78

0.76 1.10

0.99 76 N076L 0.31

0.94 1.22

0.85 76 N076M

76 N076P

76 N076Q 1.20

0.92 0.98 0.1 1.06 76 N076R 0.93

0.55 1.03

0.93 76 N076S 1.18 0.86 0.94 0.94

1.09 76 N076T 0.74

0.84 0.87

1.11 76 N076V 0.47

0.75 1.21 0.4 1.01 76 N076W 0.45

1.40 1.20

1.15 76 N076Y 0.91 0.40 0.68 0.93

1.06 77 N077A 0.21 1.14

0.27 0.2 0.06 77 N077C 0.23 0.95 0.12 0.36 0.2 0.14 77 N077D 0.44 1.02 0.96 1.05

1.00 77 N077E 0.20 1.17 0.13 0.35 0.2 0.07 77 N077F 0.20 0.90

0.20

77 N077G 0.21 1.52 0.75 0.97

0.12 77 N077H 0.20 1.16

0.38 0.2 0.09 77 N077I 0.23 0.63 0.09 0.28 0.2 0.08 77 N077K 0.18 1.28 0.06 0.36 0.2 0.12 77 N077L 0.19 2.18 0.24 0.77 0.1 0.12 77 N077M 0.21 0.94 0.11 0.32 0.3 0.06 77 N077P 0.19 2.17

0.63 0.3 0.06 77 N077Q 0.20 2.11 0.83 1.17

0.38 77 N077R 0.18 2.49 0.10 0.93 0.1 0.16 77 N077S 0.26 1.67 1.31 1.20

0.78 77 N077T 0.18 4.17 1.33 1.47

0.28 77 N077V 0.13

0.4 0.06 77 N077W 0.12

77 N077Y 0.13

0.2 0.09 78 S078A 1.21 1.08 1.10 1.03 1.1 0.91 78 S078C 1.23 1.03 0.77 0.88 1.5 0.83 78 S078D 1.33 1.10 0.83 0.88 1.7 0.90 78 S078E 1.04 1.05 0.87 0.96 1.1 0.91 78 S078F 1.11 0.95 0.64 0.98 0.5 0.97 78 S078G 1.28 1.14 0.83 0.92 0.6 0.88 78 S078H

78 S078I 1.00 1.03 0.70 0.96 0.3 0.99 78 S078K 1.25 0.98 0.62 0.94 0.3 0.92 78 S078L 0.68 1.01 0.78 0.92 0.8 0.96 78 S078M 1.03 1.06 1.09 0.99 1.2 1.04 78 S078N 1.19 1.04 0.87 1.16 1.6 1.00 78 S078P 1.25 1.00 0.93 0.94

0.95 78 S078Q 1.12 1.11 0.94 1.09 1.4 1.36 78 S078R 1.22 1.02 0.52 0.81 0.7 1.15 78 S078T 1.07 1.17 1.02 0.99 1.4 1.09 78 S078V 1.13 1.16 0.97 0.91 0.5 0.90 78 S078W 1.00 1.31 0.67 1.02 0.3 1.08 78 S078Y 1.06 0.97 0.68 1.12 0.6 1.06 79 I079A 1.26 0.63 1.14 0.93

1.13 79 I079C 1.22 0.73 1.12 1.02 0.2 0.91 79 I079D

79 I079E 1.28 0.71 1.02 0.98 0.1 1.00 79 I079F 1.23 0.93 1.22 1.03 0.9 0.95 79 I079G 0.90 0.83 1.18 0.90

0.95 79 I079H 1.21 0.60 1.11 1.10

1.03 79 I079K 1.14 0.25 0.87 0.88

0.87 79 I079L 1.20 0.84 1.14 1.08

0.91 79 I079M

79 I079N 0.92 0.76 1.03 1.17

0.89 79 I079P 0.17

1.05 0.47

79 I079Q 1.11 0.39 1.22 0.89

1.11 79 I079R 1.15 0.58 0.92 0.95

0.97 79 I079S 1.03 0.68 1.00 1.00

0.91 79 I079T 1.10 0.63 1.22 1.11

0.98 79 I079V 1.10 0.68 1.15 1.02 0.1 0.97 79 I079W 1.13 0.81 1.15 1.18 0.1 1.00 79 I079Y 1.19 0.76 1.26 0.92 1.0 1.25 80 G080A 0.16 0.78

2.12 0.1 0.16 80 G080C 0.19 0.60 1.75 1.16 0.1 0.36 80 G080D 0.18

0.40 0.10

80 G080E 0.18

0.39 0.08

80 G080F 0.22 0.81 1.58 1.12

0.61 80 G080H 0.16 11.26  32.17  3.11

0.32 80 G080I 0.17

1.18 0.12

80 G080K 0.16

0.59 1.27

80 G080L 0.15 0.37

4.69 0.1 0.11 80 G080M

80 G080N 0.15 0.92

0.73

80 G080P 0.23

0.18

80 G080Q 0.15 0.40

80 G080R 0.15 0.38

80 G080S 0.16 1.10

0.17

80 G080T 0.25

0.13

80 G080V 0.13 0.11

80 G080W 0.13

0.1 0.12 80 G080Y 0.14

0.49 81 V081A 0.66 1.15 0.91 1.16

0.80 81 V081C 1.10 1.23 0.92 0.95

0.88 81 V081D 0.24 1.35 0.77 0.60 0.1 0.14 81 V081E

81 V081F 0.91 1.32 0.89 1.08

0.80 81 V081G 0.63 1.17 0.82 1.09

0.69 81 V081H 0.72 1.45 0.96 1.04

0.73 81 V081I 1.15 1.09 0.82 1.05 0.3 0.88 81 V081K 0.45 0.86 0.60 1.19

0.82 81 V081L 1.09 1.16 0.84 1.18

0.97 81 V081M 0.94 1.16 0.75 0.99

0.89 81 V081N 0.41 1.33 0.87 1.24

0.70 81 V081P 0.20

3.63 0.1 0.15 81 V081Q 0.61 1.30 0.77 1.08

0.91 81 V081R 0.24 2.02 1.48 1.77

0.61 81 V081S 0.24 0.14

81 V081T 0.94 1.17 0.79 1.00 0.2 0.67 81 V081W 0.63 1.36 0.81 1.19

0.76 81 V081Y 0.88 1.22 0.77 1.08 0.1 0.84 82 L082A 0.63 1.22 1.02 1.09

0.81 82 L082C 0.85 1.17 0.99 0.99

0.83 82 L082D 0.25 0.06

82 L082E 0.45 1.27 1.13 1.03

0.83 82 L082F 0.56 1.12 1.13 1.15

0.94 82 L082G 0.21 2.20 1.71 1.50 0.1 0.36 82 L082H 0.67 1.17 1.07 1.12

0.85 82 L082K 0.80 0.89 0.89 1.02

1.06 82 L082M 0.98 1.16 1.03 1.04

0.98 82 L082N 0.26 1.75 1.47 1.66

0.60 82 L082P 0.30 0.06

82 L082Q 0.68 1.29 1.19 1.15

0.93 82 L082R 0.54 0.99 0.95 1.12

0.75 82 L082S 0.47 1.28 1.12 1.12

0.89 82 L082T 0.51 1.24 1.10 1.19

0.82 82 L082V 0.78 1.21 1.19 1.10 0.2 1.13 82 L082W 0.17 10.29  8.50 4.18 0.7 0.37 82 L082Y 0.59 1.18 1.21 1.25

1.15 83 G083A 0.38

83 G083C 0.35

83 G083D

83 G083E 0.38

83 G083F 0.35

83 G083H

83 G083I 0.39

83 G083K 0.34

0.08

83 G083L 0.21

0.20 0.07

83 G083M 0.37

0.10

83 G083N

83 G083P 0.39

0.07

83 G083Q 0.34

83 G083R 0.32

83 G083S 0.26 0.96 1.61 1.24

0.83 83 G083T 0.29

0.15

83 G083V 0.30

0.06

83 G083W 0.29

0.08

83 G083Y 0.14

1.1 0.33 84 V084A 1.27 0.84 0.96 0.82 0.7 1.08 84 V084C 1.15 0.77 0.75 0.79 0.8 0.97 84 V084D 0.17

0.88

84 V084E 0.19

84 V084F 0.17

0.56

84 V084G 0.29 0.75 0.84 0.86 0.5 0.66 84 V084H 0.24

84 V084I 1.08 0.96 0.99 0.68 0.5 0.99 84 V084K 0.28

0.07 0.07

84 V084L 0.51 0.66 0.91 1.00 0.3 1.07 84 V084M 0.89 0.91 0.68 0.87 0.3 1.20 84 V084N 0.67 0.75 0.98 0.88 0.8 1.09 84 V084P 0.14

84 V084Q

84 V084R 0.33

84 V084S 0.81 0.79 0.64 0.85 0.5 1.00 84 V084T 1.06 0.95 0.42 0.70 0.7 0.92 84 V084W 0.29

84 V084Y 0.20

0.25

85 A085C 0.64 0.84 0.85 0.99 0.8 0.73 85 A085D 0.23

0.18 0.07

85 A085E 0.24 0.07

85 A085F 0.36

0.08

85 A085G 0.77 0.93 0.92 0.97 0.9 0.94 85 A085I 0.17 1.69 0.66 0.71

85 A085K 0.29

0.16

85 A085L 0.21 0.10

0.06

85 A085M 0.54

85 A085N 0.25 0.08 0.06

85 A085R 0.39

85 A085S 0.90 0.94 0.94 0.97 0.9 0.93 85 A085T 0.43 1.35 1.11 0.88 0.6 0.95 85 A085V 0.20 2.50 2.45 2.31 0.7 0.49 85 A085Y 0.24 0.12

86 P086A 0.45 1.30 1.13 1.29 0.7 1.08 86 P086D 0.52 1.20 0.80 1.21 0.5 0.95 86 P086E 0.46 0.88 1.20 1.02 0.4 1.10 86 P086G 0.37 1.41 0.91 1.28 0.1 0.76 86 P086K 0.25

86 P086M 0.27 1.95 1.84 1.83 0.1 1.02 86 P086N 0.54 1.25 1.13 1.14 0.7 1.07 86 P086Q 0.25 1.54 1.60 1.99 0.1 0.88 86 P086R 0.19 3.54 3.82 2.73 0.7 0.72 86 P086S 0.53 1.15 1.15 1.06 0.7 1.21 86 P086T 0.28 1.73 1.80 1.87 0.2 1.05 86 P086V 0.16

36.35  0.1 0.19 86 P086W 0.42 1.35 1.52 1.25 0.4 1.41 86 P086Y 0.39 1.46 1.19 1.70 0.9 1.38 87 S087A 1.11 1.20 1.08 1.01 0.9 0.82 87 S087C 1.16 1.11 0.98 0.86 1.1 0.86 87 S087D 1.12 1.29 1.05 0.95 1.5 0.89 87 S087E 1.19 1.03 1.04 1.00 1.4 0.96 87 S087F 0.92 1.36 0.88 1.06 0.5 0.95 87 S087G 1.16 1.16 0.91 1.03 0.8 0.85 87 S087I 0.56 1.40 0.81 1.01 0.4 0.90 87 S087K 1.39 0.87 0.72 1.10 0.4 0.85 87 S087L 1.07 1.31 0.95 1.07 0.8 0.98 87 S087M 1.02 1.34 0.99 1.08 0.7 1.04 87 S087N 1.32 1.23 1.04 0.96 1.0 0.86 87 S087Q 0.81 1.34 0.93 0.96 0.8 0.87 87 S087R 1.23 1.06 0.73 0.99 0.2 0.82 87 S087T 1.08 1.17 1.00 1.10 0.9 1.16 87 S087V 0.92 1.33 0.95 1.17 0.9 1.15 87 S087W 0.91 1.44 1.01 1.26 0.5 1.06 88 A088C 0.78 1.12 1.30 1.05 0.9 1.02 88 A088D 0.27 1.44 1.63 1.25 0.7 0.68 88 A088E 0.17 11.44  17.45  1.68 0.6 0.16 88 A088G 0.65 1.19 1.28 1.06 0.9 1.07 88 A088K 0.21 2.38 2.98 1.68 0.8 0.67 88 A088L 0.62 1.20 1.17 0.93 0.8 1.06 88 A088M 0.45 1.03 1.50 0.98 0.4 0.73 88 A088N 0.67 0.97 1.11 1.08 0.6 1.17 88 A088P 0.21 2.19 3.40 2.03 0.9 0.62 88 A088Q 0.22 1.86 1.99 1.23 0.5 0.52 88 A088R 0.37

88 A088S 0.84 0.94 1.31 0.91 0.9 1.09 88 A088T 0.86 1.28 1.29 0.94 1.0 1.08 88 A088V 0.87 1.22 1.41 0.94 0.9 1.11 88 A088W 0.49

0.06

88 A088Y 0.18 0.66 2.48 0.40

89 S089A 0.22 0.73

89 S089C 0.91 1.14 1.14 0.99 0.9 0.92 89 S089D 1.20 1.35 1.04 1.09 0.8 0.96 89 S089E 0.92 1.07 1.17 0.95 0.8 0.93 89 S089F 0.65 1.14 1.27 0.90 0.8 1.16 89 S089G 0.88 1.13 1.10 1.13 0.8 1.04 89 S089H 0.99 0.86 1.23 1.09 0.6 1.09 89 S089I 0.26 0.29

0.11

89 S089K 0.98 0.99 1.06 1.01 0.8 0.88 89 S089L 0.41 1.08 1.52 1.40 1.3 0.93 89 S089M 0.43 1.28 1.34 1.17 1.4 0.86 89 S089N

89 S089P 0.20

0.13

89 S089Q 0.21 108.13  37.15  0.22

89 S089R 0.71 0.67 1.08 1.06 0.8 0.94 89 S089T

89 S089V 0.66 1.31 1.27 1.17 0.7 1.34 89 S089W 0.37 1.19 1.84 1.30 1.2 1.05 89 S089Y 0.75 1.22 1.34 1.00 0.7 1.13 90 L090A 0.35 1.29 1.22 1.35 0.7 0.85 90 L090D 0.20 2.40 2.05 2.19 0.6 0.47 90 L090E 0.23 1.61 1.38 1.49 1.0 0.52 90 L090F 0.30 1.57 0.81 1.39 0.3 0.34 90 L090G 0.28 0.21 0.15 0.22 0.9 0.11 90 L090H 0.23 2.00 2.18 2.26 1.0 0.88 90 L090M 0.78 1.07 1.04 0.94 1.0 0.95 90 L090P 0.27 1.56 1.73 1.61 0.9 0.88 90 L090Q 0.44 1.22 1.21 1.20 1.1 1.05 90 L090R 0.35

90 L090S 0.24 1.57 1.85 1.57 0.7 0.93 90 L090T 0.21 3.87 3.31 2.49 0.8 0.96 90 L090V 0.77 1.20 1.08 1.18 0.8 1.12 90 L090W 0.15

0.7 0.07 91 Y091A 0.25 0.60 1.29 1.22 0.9 0.67 91 Y091C 0.23 0.99 2.01 1.14 1.1 0.54 91 Y091D 0.31 0.90 1.51 1.27 1.1 0.80 91 Y091E 0.16

3.30 0.67 1.3 0.10 91 Y091F 1.07 0.60 1.21 1.23 1.1 1.00 91 Y091G 0.19

0.32 0.11 0.9 0.06 91 Y091H 0.80 0.71 1.16 1.04 1.0 0.99 91 Y091I 0.22 1.01 2.17 1.25 1.2 0.58 91 Y091K 0.22

0.06

91 Y091L 0.18 1.59 2.82 1.67 1.0 0.49 91 Y091M 0.27 1.09 1.56 1.13 1.1 0.62 91 Y091N

91 Y091P 0.31

0.09 0.48

91 Y091Q 0.16 7.64 26.89  1.98 1.2 0.25 91 Y091R 0.16

11.79  0.51 1.1 0.09 91 Y091S 0.25 0.90 1.68 1.44 0.8 0.86 91 Y091T 0.17 3.68 8.06 2.67 0.9 0.61 91 Y091V 0.23 0.89 1.92 1.46 1.0 0.70 91 Y091W 0.14 0.33

92 A092C 0.29 2.61 2.00 1.71 0.6 0.33 92 A092E 0.50

0.08

92 A092F 0.36

0.08

92 A092G 0.55 1.16 1.46 1.30 0.8 0.67 92 A092I 0.33 1.73 1.53 1.55 0.7 0.31 92 A092K 0.17

4.27 0.1 0.20 92 A092M 0.21 2.49 2.62 2.92 0.6 0.16 92 A092N 0.18 6.44 7.31 5.48 0.7 0.15 92 A092P 0.26 1.62 2.34 2.13 0.9 0.47 92 A092Q 0.28 0.08

0.07

92 A092R 0.27 0.41 0.06 0.27

92 A092S 1.04 0.85 0.94 1.22 1.1 0.87 92 A092T 0.73 1.10 1.14 0.98 0.9 0.96 92 A092V 0.30 1.40 1.31 1.73 0.6 0.50 92 A092W 0.28 0.13

0.09

93 V093A 0.31 1.09 1.32 1.22 0.9 0.68 93 V093C 0.61 1.02 1.24 1.00 0.9 0.86 93 V093D 0.21 2.38 3.40 2.01 1.1 0.67 93 V093E 0.27 0.22 0.25 0.12

93 V093F 0.22 1.32 2.23 1.46 1.0 0.61 93 V093G 0.23 0.60 1.00 0.61 1.1 0.18 93 V093H 0.48

93 V093K 0.63

93 V093L 0.58 1.39 1.12 1.01 0.8 0.98 93 V093N 0.32 0.09 0.20 0.11

93 V093P 0.34

0.19

93 V093Q 0.42 0.06

93 V093R 0.48

93 V093S 0.29 0.17 0.35 0.27 0.9 0.12 93 V093T 0.33 1.46 1.70 1.37 1.1 1.04 94 K094C 0.22 1.33 1.37 1.05 1.0 0.17 94 K094D 0.32 0.10 0.11 0.15

94 K094E 0.21 0.66 0.92 0.67 0.8 0.06 94 K094F 0.29 0.18 0.10 0.14

94 K094G 0.27 0.30 14.09  0.31

94 K094H 0.33 0.16

0.10

94 K094I 0.33

0.12 0.07

94 K094L 0.30 0.26 0.32 0.28 1.1 0.06 94 K094N 0.28 0.69 3.31 0.56 0.8 0.08 94 K094Q 0.42 1.19 1.22 0.90 1.0 0.72 94 K094R 0.41 1.36 1.48 1.32 0.8 0.39 94 K094S 0.19 4.15 3.79 2.53 1.0 0.24 94 K094T 0.14

0.8 0.19 94 K094V 0.21 0.75 1.10 0.67 0.8 0.12 94 K094W 0.44

94 K094Y 0.49

95 V095A 0.44 0.85 0.53 0.71 1.0 0.87 95 V095C 1.03 0.96 0.64 0.87 1.0 1.11 95 V095D 0.25 0.08

95 V095E 0.31 0.32 0.08

95 V095F 0.32

95 V095G 0.43 0.97 0.34 0.83 1.0 0.86 95 V095H 0.26

95 V095I 0.43 2.43 1.17 1.31

95 V095K 0.38

95 V095L 0.32 0.09

95 V095M 0.27 0.13

95 V095N 0.24 0.18

0.06

95 V095P 0.34

95 V095R 0.24 0.26 0.06

95 V095S 0.91 1.07 0.82 0.96 1.1 1.11 95 V095T 0.90 1.23 0.95 1.04 1.1 0.98 95 V095W 0.17 0.62

0.08

95 V095Y 0.25 0.19

96 L096C 0.57 1.04 0.44 0.78

96 L096D 0.26 0.13

96 L096E 0.22 0.56

96 L096F 0.45 2.00 0.80 1.35 0.9 0.55 96 L096H 0.20 1.89 0.18 0.37

96 L096I 0.76 1.64 0.85 1.02 1.2 0.35 96 L096K 0.19 0.54

0.10

96 L096M 0.91 1.53 1.09 1.23 0.9 0.46 96 L096N 0.17 6.10 0.90 0.69

96 L096P 0.22 0.38

96 L096Q 0.17 31.69  6.84 3.85

96 L096R 0.14

0.20

96 L096S 0.23 3.81 1.03 1.50

96 L096T 0.44 2.29 1.26 1.38

96 L096V 0.95 1.42 0.85 1.31 1.1 0.08 96 L096W 0.20 5.01 1.57 2.17 1.0 0.33 96 L096Y 0.30 2.01 0.73 1.18

97 G097A 0.91 1.55 0.95 1.33 1.0 0.77 97 G097C 1.01 1.66 1.07 1.08 1.0 0.49 97 G097D 1.55 1.43 0.79 1.20 1.0 0.76 97 G097E 1.14 1.38 0.78 1.06 1.1 0.71 97 G097F 0.29 1.93 1.01 1.36 0.9 0.29 97 G097H 0.85 1.26 1.10 1.01 1.0 0.47 97 G097K 1.23 1.17 0.63 1.00 1.1 0.77 97 G097L 0.77 1.43 1.11 1.24 1.1 0.70 97 G097M 0.84 1.32 1.04 1.18 1.1 0.91 97 G097P 0.39 2.35 1.56 1.34 1.1 0.69 97 G097Q 0.97 1.36 0.77 1.03 1.2 0.98 97 G097R 1.22 0.97 0.64 1.02 1.0 0.92 97 G097S 0.98 1.45 1.12 1.07 0.9 0.95 97 G097T 1.02 1.23 0.93 1.10 1.0 1.09 97 G097V 0.54 1.56 1.09 1.22 1.0 0.95 97 G097W 0.23 2.95 1.54 1.49 1.0 0.34 97 G097Y 0.37 1.37 0.93 1.04 0.9 0.34 98 A098C 1.10 0.86 1.07 1.06 1.2 0.94 98 A098D 1.18 0.87 1.36 1.19 1.2 0.91 98 A098E 1.08 0.49 1.20 1.06 0.9 1.24 98 A098F 0.73 0.54 1.00 1.02 1.0 1.16 98 A098G 1.20 0.94 1.27 1.09 0.9 0.93 98 A098H 1.26 0.70 1.08 0.97 1.0 0.99 98 A098I 0.98 0.93 1.00 1.08 0.9 1.39 98 A098K

98 A098L 0.96 0.63 1.09 1.01 1.0 1.05 98 A098M

98 A098N 0.32

98 A098P 1.13 0.87 1.19 1.09 1.0 0.79 98 A098Q 0.89 0.76 1.13 1.05 1.0 1.09 98 A098R 1.22 0.70 1.00 1.11 1.0 0.95 98 A098S 1.20 0.85 1.12 1.12 0.8 1.01 98 A098T 0.98 0.74 1.09 0.99 1.0 1.36 98 A098V 0.99 0.91 1.17 0.97 0.9 1.70 98 A098W

98 A098Y 0.89 0.75 1.20 1.01 0.8 1.37 99 D099A 0.81 1.07 0.65 1.04 0.8 0.62 99 D099C 0.71 1.49 0.78 1.08 1.1 0.62 99 D099E 1.04 1.37 0.80 1.03 1.0 0.80 99 D099F 0.50 1.14 0.53 1.08 1.0 0.44 99 D099H 0.79 1.17 0.53 0.98 0.9 0.65 99 D099I 0.44 1.59 0.64 1.10 1.0 0.55 99 D099K 0.94 0.72 0.43 1.00 1.0 0.75 99 D099L 0.34 1.20 0.47 0.93 1.1 0.57 99 D099M 0.59 1.38 0.65 1.18 0.9 0.66 99 D099N 1.06 1.09 0.74 0.99 1.1 0.88 99 D099P 0.39 1.98 0.89 1.21 1.0 0.40 99 D099Q 0.98 1.08 0.77 1.15 1.0 0.65 99 D099R 0.87 0.54 0.42 0.86 1.1 0.83 99 D099S 0.87 1.00 0.60 0.97 0.9 0.94 99 D099T 0.70 1.08 0.70 1.10 0.9 0.97 99 D099V 0.43 1.71 0.75 1.08 0.9 0.61 99 D099W 0.58 1.22 0.57 0.89 0.8 0.88 99 D099Y 0.50 1.43 0.60 1.07 0.9 0.60 100 G100A 0.94 0.95 1.13 0.96 1.0 0.35 100 G100C

100 G100D 0.77 1.41 1.35 1.08 0.9 0.34 100 G100E 0.54 1.66 1.46 1.25 1.0 0.30 100 G100F 0.53 1.04 1.32 1.22 0.9 0.10 100 G100H 0.55 1.41 1.18 1.05 0.9 0.28 100 G100I 0.28 1.80 1.64 1.21

100 G100K 0.65 1.46 1.00 1.22 0.9 0.31 100 G100L 1.23 1.17 0.89 0.97

100 G100M 1.13 1.42 1.16 1.20 0.8 0.17 100 G100N 1.09 1.25 1.29 1.31 1.0 0.41 100 G100P 0.40

0.10

100 G100Q 0.66 1.57 1.18 1.38 1.0 0.35 100 G100R 0.68 1.09 0.89 1.03 0.9 0.29 100 G100S 0.79 1.28 1.35 1.15 0.9 0.35 100 G100T 0.34 2.17 1.64 1.46 1.0 0.18 100 G100V 0.31 1.98 1.55 1.39 1.0 0.07 100 G100W 0.50 0.92 0.90 1.04

100 G100Y 0.49 1.58 1.27 1.05 1.0 0.20 101 S101A 1.27 1.38 1.00 1.09 1.1 1.08 101 S101C 1.24 1.14 0.67 0.90 1.2 0.61 101 S101E 1.35 1.52 1.19 1.14 1.1 0.71 101 S101F 0.96 1.02 0.73 0.97 1.0 1.13 101 S101G 0.38 1.30 0.46 0.67 1.1 0.21 101 S101I 1.01 1.22 0.75 0.86 1.2 0.91 101 S101K 1.28 1.15 0.62 1.00 1.1 0.99 101 S101L 1.10 1.21 0.80 1.00 1.0 1.21 101 S101M 1.01 1.22 0.79 1.08 1.1 1.21 101 S101N 1.24 1.46 0.99 1.10 1.1 1.03 101 S101P 0.25 3.64 1.39 1.83 1.1 0.30 101 S101Q 0.59 1.56 0.79 1.05 1.0 1.24 101 S101R 1.20 1.04 0.65 0.90 1.0 0.94 101 S101T 0.94 1.34 0.68 1.16 1.0 1.12 101 S101V 0.92 1.39 0.74 1.18 0.9 1.19 101 S101Y 0.72 1.04 0.48 0.92 1.0 1.54 102 G102A 1.12 1.46 1.31 1.19 1.0 0.31 102 G102C 0.82 0.99 0.39 0.74

102 G102E 0.25

102 G102F 0.21 0.30

0.07

102 G102I 0.23 1.13 0.16 0.09

102 G102K 0.23 0.14

102 G102L 0.20 0.12

102 G102M 0.24 0.30 0.11

102 G102N 0.22 1.24 0.09 0.08

102 G102R 0.20 0.25

102 G102S 0.77 1.61 1.10 1.04 1.1 0.11 102 G102V 0.21 0.69

102 G102W 0.21 0.25

102 G102Y 0.29 0.15

103 Q103A 1.09 0.93 0.93 0.89 1.0 0.92 103 Q103C 1.19 1.10 1.05 0.97 1.0 0.63 103 Q103E 1.21 1.38 1.15 1.05 1.0 0.64 103 Q103F 1.02 0.82 0.57 0.83 0.9 0.91 103 Q103G 0.39 1.48 1.06 1.34 1.1 0.43 103 Q103H 0.89 1.35 0.89 0.93 0.9 0.65 103 Q103I 1.06 0.88 0.89 0.87 1.1 0.82 103 Q103K 0.17 2.63 1.36 1.25 1.0 0.45 103 Q103L 0.44 0.87 0.68 0.81 1.1 0.93 103 Q103M 0.89 1.06 0.76 0.99 0.9 1.01 103 Q103N 1.44 1.44 1.23 0.88 1.0 0.74 103 Q103R 1.09 0.47 0.57 0.88 1.1 1.04 103 Q103S 1.21 1.03 0.96 0.91 1.0 1.07 103 Q103T 0.84 1.01 0.94 0.95 1.0 0.89 103 Q103V 0.94 1.13 1.03 0.97 1.0 0.75 103 Q103W 0.98 0.65 0.63 0.73 1.1 0.76 104 Y104A 0.37 0.90 1.00 1.03

104 Y104C 0.34 1.24 1.33 1.31 1.1 0.06 104 Y104F 0.90 0.88 0.78 1.03 1.0 0.67 104 Y104G 0.27 0.18 0.09 0.33

104 Y104H 0.75 0.95 1.78 0.95 1.1 0.30 104 Y104I 0.30 1.10 1.10 1.48 1.3 0.08 104 Y104K 0.43

104 Y104L 0.24 1.45 1.48 1.17

104 Y104M 0.31 1.53 1.50 1.27 1.2 0.08 104 Y104N 0.46 1.42 1.78 1.04 1.1 0.10 104 Y104P 0.48

104 Y104Q 0.41

0.34

104 Y104R 0.34 0.11

0.07

104 Y104S 0.27 1.29 1.46 1.08

104 Y104T 0.42 1.33 1.69 1.35 2.0 0.08 104 Y104V 0.30 1.73 1.19 1.43

104 Y104W 0.62 0.82 0.89 1.17 1.2 1.38 105 S105A 0.67 1.06 0.97 1.01 1.0 1.16 105 S105C 0.32 0.91 1.10 0.81 1.1 0.52 105 S105D 0.39 1.33 1.03 1.21 1.1 0.90 105 S105E 0.54 0.98 0.79 0.93 1.2 0.76 105 S105F 0.23

0.06 0.08

105 S105G 0.68 1.12 0.98 0.98 0.9 0.93 105 S105H

105 S105I 0.19 1.60 1.06 0.72 1.0 0.26 105 S105K 0.21 0.13 0.10 0.13 1.2 0.09 105 S105L 0.17 0.60 9.45 0.53 1.2 0.12 105 S105M 0.18 1.09 1.67 1.11 0.9 0.19 105 S105N 0.32 1.10 0.97 1.17 1.1 0.81 105 S105P 0.24

105 S105Q 0.24 0.70 0.76 0.72 1.0 0.40 105 S105R 0.16 3.02 3.37 0.95 1.2 0.19 105 S105T 0.87 1.19 1.11 1.21 1.0 1.07 105 S105V 0.18 2.82 3.06 2.81 1.0 0.75 105 S105W 0.14

1.0 0.22 105 S105Y 0.18 0.07 0.43 0.06

106 W106A 0.38 1.42 1.15 1.06 0.9 0.36 106 W106C 0.37 1.38 1.10 0.99 0.9 0.23 106 W106D

106 W106E 0.39 1.73 1.34 1.15 1.1 0.35 106 W106F 0.81 1.33 0.80 1.29 1.0 0.40 106 W106G 0.24 1.40 1.28 1.21 0.9 0.12 106 W106H 0.78 1.02 0.97 1.16 0.9 0.72 106 W106I 0.30 1.51 1.13 1.34 1.1 0.40 106 W106K 0.49

106 W106L 0.31 1.56 1.11 1.40 1.1 0.26 106 W106M 0.41 1.36 1.11 1.13 0.9 0.30 106 W106N 0.51 1.16 1.02 1.23 1.0 0.51 106 W106P 0.36

0.06

106 W106Q

106 W106R 0.34 0.94 1.24 1.26 1.0 0.34 106 W106S 0.37 1.41 0.93 1.19 2.0 0.18 106 W106T 0.39 1.41 1.15 1.25 0.9 0.30 106 W106V 0.33 1.48 1.20 1.19 0.9 0.49 106 W106Y 0.90 1.19 1.05 1.22 0.9 0.43 107 I107E 0.47 1.07 1.99 1.00 1.0 0.95 107 I107F 0.54 0.87 0.79 1.16 1.0 0.06 107 I107G 0.27 0.82 0.43 0.72

107 I107H 0.52 0.11 0.15 0.07

107 I107K 0.50

107 I107L 0.84 0.57 0.33 0.48 1.0 0.95 107 I107M 0.86 1.18 2.50 0.93 1.0 0.17 107 I107N 0.40 0.72 0.61 0.49

107 I107Q 0.50 0.76 0.68 0.67

107 I107R 0.23 2.33 2.34 1.86 1.2 0.06 107 I107S 0.46 1.41 0.88 1.22 1.0 0.08 107 I107T 0.70 1.35 2.33 0.93 1.0 0.13 107 I107V 0.82 0.71 0.73 0.78 0.9 1.33 107 I107W 0.61 1.28 1.47 1.05

107 I107Y 0.39 0.27 0.47 0.37

108 I108A 0.38 1.15 1.22 1.17 0.8 0.70 108 I108C 0.79 1.09 1.19 1.00 0.9 0.76 108 I108D 0.32

0.06

108 I108E 0.21 0.23 1.19 0.59 0.9 0.13 108 I108F 0.26 0.18 0.23 0.09

108 I108G 0.21

0.36 0.11

108 I108H 0.29

0.07

108 I108K

108 I108L 0.73 1.29 1.29 1.05 1.0 0.41 108 I108M 0.80 1.10 1.21 1.10 0.7 0.73 108 I108N 0.20 0.34 0.24 0.14

108 I108P 0.22

0.29

108 I108Q 0.20 0.33 0.24 0.07 0.7 0.06 108 I108R 0.29

0.06

108 I108S 0.16 2.38 8.60 1.30 0.9 0.13 108 I108T 0.30 1.75 1.66 1.51 0.9 0.77 108 I108V 1.11 1.29 1.09 1.16 1.0 0.93 108 I108W 0.28

0.07

108 I108Y 0.22 0.32 0.15

109 N109A 0.62 1.05 1.01 1.09 1.1 1.03 109 N109C 0.90 0.82 0.73 0.89 1.1 0.85 109 N109D

109 N109E 0.66 0.94 1.01 1.05 1.1 1.09 109 N109F 0.52 1.17 0.79 1.20 1.1 0.97 109 N109G 0.66 1.13 0.93 1.01 1.1 1.12 109 N109H 0.93 1.01 0.64 1.04 1.1 0.92 109 N109I

109 N109K

109 N109L 0.81 0.80 0.99 1.18 1.1 1.17 109 N109M 0.20

0.36 0.24 1.0 0.07 109 N109P 0.59 1.13 0.94 1.20 1.0 0.79 109 N109Q 1.04 0.63 0.55 0.99 1.2 0.93 109 N109R 0.71 0.58 0.57 1.03 1.0 1.07 109 N109S 1.03 0.93 0.90 1.13 1.0 1.05 109 N109T 0.94 1.26 0.82 1.02 0.9 1.09 109 N109V 0.59 0.91 0.91 1.17 1.0 1.08 109 N109W 0.63 0.92 0.76 1.15 0.9 0.92 109 N109Y 0.54 0.88 0.89 1.08 0.9 0.96 110 G110A 0.79 1.28 0.75 1.05 0.9 0.78 110 G110C 0.41

110 G110D 0.53

110 G110E 0.53

2.02

110 G110F 0.53

1.55

110 G110H 0.45

0.06

110 G110I 0.47

110 G110K 0.48

110 G110L 0.48

0.40

110 G110M 0.49 0.06 0.53

110 G110N 0.51

110 G110P 0.48

0.08

110 G110R 0.50

0.94

110 G110S 0.25 2.17 1.37 1.69 0.9 0.51 110 G110T 0.20 4.57 3.95 2.82 0.9 0.53 110 G110Y 0.44

111 I111A 0.24 3.80 2.39 1.92 0.9 0.30 111 I111C 0.36 1.88 1.45 1.48 0.9 0.88 111 I111D 0.24 0.38 0.07

111 I111E 0.22 0.52 0.21 0.06

111 I111F 0.46 1.68 1.11 1.24

111 I111G 0.29 0.19

111 I111H 0.25 0.36

0.06

111 I111K 0.22 0.60 0.29 0.10

111 I111L 1.00 1.30 0.96 1.10 1.0 0.74 111 I111M 0.80 1.37 0.98 1.04 1.1 0.74 111 I111N 0.21

0.18

111 I111P 0.25 0.24 0.18 0.07

111 I111Q 0.19

111 I111R 0.25 0.17 0.12 0.12

111 I111S 0.18

111 I111T 0.31 3.10 1.56 1.67 1.0 0.85 111 I111V 0.73 1.59 0.98 1.32 1.0 0.83 111 I111W 0.21

0.13

111 I111Y 0.20

1.39

112 E112A 0.33 1.05 0.84 1.31 1.1 0.77 112 E112C 0.49 0.40 0.28 0.28 1.1 0.20 112 E112D 0.97 1.20 0.97 1.11 1.0 0.91 112 E112F 0.17

1.0 0.24 112 E112G 0.37 0.87 0.64 0.90 1.0 0.56 112 E112H

112 E112I 0.22 7.24 2.74 2.71 1.1 0.63 112 E112K

112 E112L 0.21 19.65  11.59  3.83 1.1 0.57 112 E112M 0.35 0.98 0.74 1.07 1.0 0.71 112 E112N 0.38 1.24 0.85 1.19 1.0 0.93 112 E112P 0.27 0.26

112 E112Q 0.39 1.25 1.01 1.27 1.0 0.97 112 E112R 0.18

1.1 0.28 112 E112S 0.38 1.22 0.98 1.05 1.0 0.85 112 E112T 0.25 2.89 2.14 1.98 1.0 0.90 112 E112V 0.21

2.81 1.1 0.35 112 E112W 0.15

1.0 0.47 112 E112Y 0.19

1.0 0.68 113 W113A 0.23

0.24 0.17 1.0 0.08 113 W113C 0.19 0.36 1.25 1.25 1.0 0.19 113 W113D 0.18 0.52 1.67 0.60 0.9 0.16 113 W113E 0.19 0.26 1.58 0.31 0.9 0.16 113 W113F 0.50 0.97 1.02 1.03 0.9 0.96 113 W113G 0.31

0.07

113 W113H 0.22 1.45 1.69 1.49 1.1 0.57 113 W113I

113 W113K 0.22

113 W113L 0.19

0.35 0.17 1.1 0.08 113 W113M 0.19 0.40 1.19 0.61 0.9 0.18 113 W113N 0.17 0.74 2.31 0.88 0.9 0.22 113 W113P 0.32

113 W113Q 0.19

0.38 0.07

113 W113R 0.22

0.08

113 W113S 0.19

0.30 0.24 1.0 0.09 113 W113T 0.17 0.12 1.00 0.51 1.1 0.10 113 W113V 0.15 0.34

1.0 0.14 113 W113Y 0.91 0.82 1.25 1.02 1.1 0.89 114 A114C 0.87 1.18 1.38 1.17 1.0 1.19 114 A114D 0.39

114 A114E 0.48

114 A114F 0.63

114 A114G 0.72 1.15 1.41 1.31 1.1 1.14 114 A114H 0.26 0.16

0.15

114 A114I 0.19 3.35 2.63 2.54 0.9 0.42 114 A114K 0.51

114 A114L 0.51

114 A114N 0.33

114 A114P 0.28 0.07

0.06

114 A114Q 0.47

114 A114R 0.45 0.09

114 A114S 0.33 1.15 1.39 1.63 1.0 0.98 114 A114T 0.59 1.03 1.49 1.53 0.9 1.46 114 A114V 0.31 1.57 2.18 1.56 0.9 0.97 114 A114W 0.40

114 A114Y 0.51

115 I115A 0.40 1.58 0.99 1.09 0.9 0.79 115 I115C 0.69 1.23 0.81 1.25 1.0 1.10 115 I115D 0.20

9.72 1.1 0.28 115 I115E 0.28 2.29 1.67 1.56 0.9 0.69 115 I115F 0.30 1.99 1.22 1.37 0.9 0.61 115 I115G 0.17

1.1 0.21 115 I115H 0.24 4.85 2.46 2.39 0.9 0.52 115 I115K 0.18

0.1 0.25 115 I115L 0.83 1.04 0.96 1.08 1.1 1.06 115 I115M 0.89 1.46 1.03 1.09 1.0 0.94 115 I115N 0.21 8.31 8.40 2.63 1.0 0.37 115 I115P 0.21 1.81 0.08 0.17

115 I115Q 0.58 1.30 0.80 1.24 1.0 1.00 115 I115R 0.38 1.37 1.00 1.21 1.0 0.86 115 I115S 0.24 4.20 2.44 2.22 0.9 0.70 115 I115T 0.59 1.46 0.89 1.08 0.9 0.91 115 I115V 0.84 1.44 0.99 1.25 0.9 1.58 115 I115W 0.16

0.9 0.34 115 I115Y 0.24 4.81 4.07 2.48 0.9 0.79 116 A116C 1.15 0.85 1.06 0.90 1.0 0.95 116 A116D 1.24 1.02 0.81 1.03 1.0 1.11 116 A116E 1.16 1.21 1.09 0.89 1.0 1.08 116 A116F 0.95 1.06 0.92 0.94 1.0 1.01 116 A116G 0.66 0.94 1.01 0.97 1.0 1.08 116 A116H 1.07 1.09 0.92 1.13 1.0 1.30 116 A116I 0.95 0.82 1.04 1.13 1.0 1.05 116 A116K 1.18 0.74 0.79 1.13 1.0 0.94 116 A116L 0.82 1.05 0.89 0.83 1.0 0.98 116 A116M 1.11 0.86 1.14 0.85 1.0 0.98 116 A116N 0.99 0.97 0.88 1.10 1.0 1.15 116 A116P 0.14

1.0 0.34 116 A116Q 1.07 0.85 0.71 1.03 1.0 1.15 116 A116R 1.15 0.86 0.73 1.09 1.0 1.15 116 A116S 1.14 1.07 0.98 1.17 0.9 1.11 116 A116T 1.03 1.01 1.12 1.06 0.9 1.17 116 A116V 0.88 1.03 1.03 0.96 1.0 1.09 116 A116W 0.86 1.24 0.71 0.97 1.0 1.17 116 A116Y 0.88 0.89 1.03 0.93 0.9 1.19 117 N117A

117 N117C 0.60 1.00 0.98 1.07 1.0 1.06 117 N117D

117 N117E 0.52 0.97 1.03 1.06 1.0 1.18 117 N117F 0.40 1.04 1.21 1.17 0.9 1.33 117 N117G 0.67 1.18 0.85 1.29 1.1 0.96 117 N117H

117 N117I 0.15

5.36 1.0 0.27 117 N117K 0.22 1.91 1.91 1.80 1.0 0.88 117 N117L 0.30 1.13 1.22 1.39 1.0 1.13 117 N117M 0.57 1.09 1.21 1.12 1.0 1.24 117 N117P 0.32

117 N117Q 1.04 0.69 0.95 0.99 1.1 1.10 117 N117R 0.80 0.98 0.78 0.98 1.0 0.90 117 N117S 0.53 1.18 1.24 1.06 1.3 1.14 117 N117T 0.80 1.05 1.07 1.15 1.0 1.13 117 N117V 0.17 5.36 4.11 2.10 1.0 0.46 117 N117W 0.25 2.09 1.77 1.63 1.0 1.05 117 N117Y 0.45 0.99 0.89 1.22 1.0 0.98 118 N118A 0.71 0.58 0.84 0.95 1.0 1.14 118 N118C 0.74 0.61 1.01 0.63 1.1 0.94 118 N118D 1.12 0.67 1.05 0.86 1.2 1.01 118 N118E 0.88 0.71 0.70 0.69 1.1 1.16 118 N118F 0.34 1.02 1.31 0.93 1.0 1.07 118 N118G 1.07 0.83 0.50 0.79 0.9 0.92 118 N118H 1.18 0.75 0.88 0.92 1.0 1.07 118 N118I 0.17 4.85 5.90 1.96 1.1 0.62 118 N118K 1.17 0.80 0.81 0.81 1.1 0.95 118 N118L 0.23 1.45 1.85 1.32 1.0 1.13 118 N118M 0.49 0.87 0.99 1.06 1.0 1.17 118 N118P 0.18

0.13 0.06

118 N118Q 1.03 0.62 1.12 0.90 1.1 1.09 118 N118R 1.35 0.82 0.62 0.80 1.0 1.01 118 N118S 0.89 0.77 0.81 0.76 0.9 1.07 118 N118T 0.64 0.72 0.86 1.08 0.9 1.21 118 N118V 0.23 1.35 1.92 1.53 1.0 0.99 118 N118W 0.27 1.16 1.36 1.41 1.1 1.03 118 N118Y 0.84 0.98 0.72 0.70 1.0 1.13 119 M119A 0.75 1.01 1.16 1.01 0.8 0.85 119 M119C 0.86 1.01 1.16 0.95 1.0 0.99 119 M119D 0.25 0.21 0.49 0.19

119 M119E 0.27

0.11 0.08

119 M119F 0.29 1.64 1.87 1.60 1.3 0.78 119 M119G 0.26 0.33 0.48 0.28 1.0 0.11 119 M119H 0.30 1.19 1.46 1.22 1.1 0.67 119 M119I 0.74 1.20 1.16 0.94 1.1 0.97 119 M119K 0.33 0.07

0.07

119 M119L 0.65 1.17 1.19 0.82 1.0 0.98 119 M119N 0.23 1.95 2.59 1.79 1.1 0.83 119 M119P 0.31 0.13 0.18 0.09

119 M119R 0.43

0.07

119 M119S 0.53 1.19 1.30 0.87 0.8 1.04 119 M119T 0.46 1.25 1.32 1.03 1.0 1.43 119 M119V 0.75 0.95 1.13 0.91 0.7 1.14 119 M119W 0.22 0.16 0.13 0.11

119 M119Y 0.15

1.0 0.28 120 D120A 1.01 1.11 0.84 0.80 1.0 0.85 120 D120C 0.67 0.84 0.95 0.76 1.0 0.92 120 D120E 1.04 0.60 0.87 1.04 1.1 0.99 120 D120F 0.24 0.50 1.07 0.78 1.0 0.50 120 D120G 1.00 0.99 1.04 0.97 0.8 0.92 120 D120H 1.13 1.07 1.16 0.88 1.1 0.93 120 D120I 0.20 0.92 1.69 1.26 1.0 0.55 120 D120K 1.15 0.88 1.01 0.95 1.1 0.81 120 D120L 0.33 0.65 1.25 1.12 1.1 0.88 120 D120M 0.73 0.87 0.97 0.95 0.7 0.93 120 D120N 1.11 1.01 1.00 0.92 1.1 0.90 120 D120P 0.22 1.12 1.61 1.14 1.1 0.53 120 D120Q 1.05 1.21 1.09 0.96 1.1 0.87 120 D120R 1.03 0.86 0.97 1.10 0.9 0.93 120 D120S 1.01 0.94 1.16 0.86 1.0 0.97 120 D120T 0.77 1.08 1.09 1.00 1.0 1.06 120 D120V 0.32 1.13 1.21 0.64 1.1 0.81 120 D120W 0.32 1.10 1.44 1.19 1.1 0.95 120 D120Y 0.22 1.30 1.73 1.29 1.0 0.70 121 V121A 0.37

121 V121C 0.76 0.98 0.99 0.78 1.1 0.92 121 V121D

121 V121E 0.19 0.45 1.16 0.85 0.7 0.21 121 V121F 0.18 0.12 1.14 0.47 0.7 0.12 121 V121G 0.18 0.14 0.37 0.34

121 V121H 0.30

121 V121I 1.15 0.83 0.88 0.81 1.0 0.89 121 V121K

121 V121L 0.81 0.95 0.91 0.88 0.8 0.94 121 V121M

121 V121N 0.25

0.14

121 V121P 0.32

0.06

121 V121Q 0.25

0.11

121 V121R 0.20

0.65 0.08

121 V121S 0.15

1.1 0.47 121 V121T 0.26 1.28 1.66 1.24 1.1 0.85 121 V121W 0.26

121 V121Y 0.30

122 I122A 0.92 1.06 1.04 1.00 0.8 0.88 122 I122C 0.78 1.17 1.22 1.09 0.8 0.98 122 I122D 0.18

122 I122E 0.17

122 I122F 0.37 1.16 1.45 1.19 1.4 0.66 122 I122G 0.20

4.05 2.3 0.36 122 I122H 0.16

122 I122K 0.23 0.86 0.47 0.12

122 I122L 0.73 0.99 1.28 1.09 0.8 0.97 122 I122M 0.93 1.17 1.05 1.23 0.8 0.96 122 I122N 0.17

122 I122P 0.25 0.15 0.25

122 I122Q 0.15

2.3 0.15 122 I122R 0.21 2.78

122 I122S 0.22 6.46 6.12 2.56 1.9 0.43 122 I122T 0.34 1.78 1.79 1.13 1.4 0.90 122 I122V 0.80 1.14 1.39 1.13 0.7 1.09 122 I122W 0.16

122 I122Y 0.16

1.9 0.55 123 N123A 0.75 1.71 1.36 1.06

123 N123C 0.95 1.53 1.35 1.43 0.5 0.09 123 N123D 0.53 1.03 1.07 1.04

123 N123E 0.96 1.13 0.77 0.94

123 N123F 0.39

0.17

123 N123G 0.47 1.81 1.59 1.34 0.4 0.13 123 N123H

123 N123I 0.55 1.20 1.11 1.06

123 N123K 0.39

123 N123L 0.87 0.98 1.13 1.06

123 N123M 0.43 1.24 1.01 0.96

123 N123P 0.36

0.13

123 N123Q 0.87 1.22 1.30 1.03 0.7 0.09 123 N123R 0.34

0.10

123 N123S 0.92 1.31 1.15 1.08 0.2 0.09 123 N123T 0.94 1.20 1.41 0.93 0.4 0.13 123 N123V 0.89 1.27 1.32 1.25

123 N123W 0.30 0.06 0.07

123 N123Y 0.29

0.09

124 M124A 0.61 1.44 1.02 0.97 1.0 0.69 124 M124C 0.26 0.86 0.54 0.63 1.3 0.07 124 M124D 0.22 0.22

124 M124E 0.23 0.59 0.08 0.13

124 M124F 1.13 1.02 0.86 1.06 0.9 0.34 124 M124H 0.20 1.36 0.26 0.31

124 M124I 1.36 1.12 1.08 1.12 1.0 0.34 124 M124K 0.18 0.15

124 M124L 0.86 0.69 1.01 1.03 1.2 0.92 124 M124N 0.18 2.98 0.78 0.79

124 M124P 0.20 0.36 0.22 0.08

124 M124Q 0.18 5.22 2.64 1.40

124 M124R 0.19 0.51

124 M124S 0.28 2.79 1.44 1.52 0.9 0.12 124 M124T 0.49 1.82 1.32 1.35 0.9 0.23 124 M124V 1.07 1.37 1.15 1.06 0.9 0.31 124 M124W 0.20 0.28

124 M124Y 0.20 0.71 1.12 0.13

125 S125A 0.92 1.90 1.40 1.17 1.1 0.06 125 S125C 1.04 0.19

0.11

125 S125D

125 S125E 0.25 0.23

125 S125F 0.22 0.96

0.08

125 S125G 0.33 0.23

0.18

125 S125H

125 S125I 0.36 0.08

125 S125K 0.23 0.21 0.10 0.06

125 S125L 0.23 0.46

125 S125M 0.24 0.49 0.18

125 S125N 1.11

125 S125P 0.48

125 S125Q 0.37 0.08

125 S125R 0.22 0.44 0.07 0.11

125 S125T 0.56 0.07

125 S125V 0.20

0.11 0.07

125 S125W 0.21 0.96 0.27

125 S125Y

126 L126A 0.93 1.56 1.09 1.22

126 L126C 1.32 0.64 0.37 0.77

126 L126D 0.23 0.08 0.07

126 L126I 1.11 1.17 1.03 1.17 1.1 0.11 126 L126K 0.14

126 L126N 0.37 1.14 0.23 0.67

126 L126P 0.28 0.07

126 L126Q 0.25 3.05 0.91 1.13

126 L126R 0.20 0.28

126 L126S 0.73 1.56 0.93 0.86

126 L126T 0.53 2.41 1.47 1.40

126 L126V 1.09 1.26 1.34 1.32 1.0 0.08 126 L126W 0.89 0.71 0.79 0.78 0.9 0.06 126 L126Y 0.58 1.47 1.10 1.27

127 G127A 1.44 0.91 0.93 0.94

127 G127C 1.06 1.00 0.57 0.87

127 G127E 0.91 0.80 0.90 0.93

127 G127F 1.20 0.60 0.31 0.68

127 G127I 1.33 0.78 0.54 0.60

127 G127K 0.58 0.70 0.47 0.88

127 G127L 0.91 0.99 0.64 0.56

127 G127M 0.93 0.84 0.57 0.83

127 G127N 1.06 1.03 0.81 0.82

127 G127P 0.41

127 G127Q 1.00 1.02 0.87 0.85

127 G127R 0.62 0.55 0.34 0.71

127 G127S 1.06 1.10 0.80 0.93

127 G127T 0.80 1.07 0.89 0.88

127 G127V 1.07 0.81 0.68 0.75

127 G127W 1.48 0.55 0.27 0.50

127 G127Y 1.00 0.68 0.54 0.60

128 G128A 1.21 1.24 1.28 1.21 1.0 0.16 128 G128C

128 G128E 0.31 1.63 1.19 1.45

128 G128F 0.50 0.70 0.46 0.80

128 G128H 0.86 1.15 1.12 0.98

128 G128I 0.39 0.35 0.21 0.36

128 G128K 0.45 0.25 0.08 0.33

128 G128L 0.57 0.29 0.16 0.37

128 G128N 0.55 1.59 1.55 1.29

128 G128P 0.39 0.17 0.12 0.18

128 G128Q 0.39 1.05 0.84 0.92

128 G128R 0.39 0.28 0.18 0.33

128 G128S 1.35 1.17 1.12 1.09 1.2 0.26 128 G128T 0.28 2.16 2.42 1.63

128 G128V 0.36 0.47 0.39 0.52

128 G128W 0.37 0.33 0.15 0.48

128 G128Y 0.39 0.24 0.16 0.36

129 P129A 1.04 1.02 0.98 0.99 0.7 0.80 129 P129C 1.37 1.09 1.11 0.91 0.9 0.56 129 P129D 1.48 1.03 1.08 0.84 1.1 0.67 129 P129E 1.42 1.24 1.04 1.10 1.0 0.87 129 P129F 0.65 1.10 0.71 1.00 0.7 1.27 129 P129G 0.78 0.82 0.60 0.81 0.8 0.56 129 P129H 0.66 0.92 0.73 0.84 0.9 0.81 129 P129I 1.14 0.95 0.99 1.11 0.9 0.40 129 P129K 1.13 0.72 0.64 1.01 0.9 1.22 129 P129L 1.12 1.13 1.21 1.06 0.9 0.53 129 P129M 1.20 1.08 0.92 1.20 0.9 0.88 129 P129N 0.90 1.00 1.04 0.98 0.9 0.85 129 P129Q 1.10 1.22 0.90 1.01 1.0 0.98 129 P129R 0.74 0.73 0.75 0.87 0.9 1.01 129 P129S 1.07 0.99 0.87 0.98 0.9 0.84 129 P129T 1.13 1.29 1.17 1.09 0.9 1.06 129 P129V 0.72 1.41 1.26 1.09 0.8 0.75 129 P129W 0.38 0.97 0.79 1.18 0.4 1.18 129 P129Y 0.71 1.01 0.90 1.04 0.8 1.56 130 S130A 1.14 0.92 0.76 0.86 1.0 0.92 130 S130C 1.24 0.75 0.95 0.66 1.1 0.78 130 S130D

130 S130E 1.36 0.73 1.29 1.03 1.1 0.88 130 S130F 1.17 0.89 0.79 0.84 1.0 1.02 130 S130G 0.93 0.95 0.99 0.98 0.9 0.80 130 S130H 1.33 0.76 0.97 1.05 1.1 1.03 130 S130I 1.22 0.82 0.97 0.91 1.1 0.95 130 S130K 1.27 0.63 0.70 0.67 1.1 1.12 130 S130L 1.04 0.90 0.79 0.80 1.1 0.98 130 S130M 1.19 0.97 0.91 0.89 0.9 0.92 130 S130N

130 S130P 0.60 1.32 1.32 1.00 0.7 0.07 130 S130Q 1.19 0.98 0.95 0.93 1.1 1.06 130 S130R 1.12 0.47 0.63 0.77 1.1 1.11 130 S130T 1.16 1.08 1.10 0.95 0.9 1.19 130 S130V 1.13 0.98 0.96 0.91 1.0 1.07 130 S130W 0.73 0.60 0.81 0.86 0.8 0.89 130 S130Y 1.24 0.73 0.94 0.95 1.0 1.04 131 G131A 1.21 0.53 1.00 0.84 1.1 1.02 131 G131C 0.55 0.59 0.82 0.83 0.6 0.87 131 G131D 0.93 0.50 0.80 0.78 0.9 1.32 131 G131E 0.35

0.34 0.64 0.9 0.67 131 G131F 0.23 0.42 0.55 0.67 0.2 0.43 131 G131H

131 G131I 0.17

0.52 0.29 1.1 0.26 131 G131K 1.00 0.48 1.00 0.89 1.0 1.39 131 G131L 0.27

0.20

131 G131M 0.53 0.47 0.89 0.75 0.6 0.90 131 G131N 0.46 0.23 0.49 0.54 0.8 1.11 131 G131P 0.22 0.77 1.29 1.21 0.1 0.50 131 G131Q 0.28 0.49 1.15 0.95 0.3 0.70 131 G131R 0.19 0.97 2.04 1.64 0.1 0.59 131 G131S 0.21 0.12 0.47 0.83 0.2 0.45 131 G131T 0.86 0.52 1.16 0.89 1.0 1.03 131 G131V 0.51 0.50 0.83 0.94 0.7 0.99 131 G131W

131 G131Y 0.30 0.26 0.40 0.71 0.9 1.04 132 S132A 0.60 1.01 1.03 1.03 0.5 0.77 132 S132C 1.25 1.06 1.10 0.83 1.0 0.64 132 S132D

132 S132E 0.33 1.04 1.40 1.01 0.9 0.50 132 S132F 0.30

0.10 0.08

132 S132G 0.83 0.83 0.14 0.94 1.0 0.41 132 S132H

132 S132I 0.25 1.62 1.82 1.25 0.8 0.57 132 S132K 0.19 0.09 0.60 0.16 0.7 0.11 132 S132L 0.25 1.27 1.65 1.22 0.8 0.78 132 S132M 0.35 1.01 1.05 1.05 0.6 0.72 132 S132N 0.88 1.38 1.35 1.17 1.0 0.87 132 S132P 0.17 9.36 11.70 2.50 1.0 0.23 132 S132Q 0.34 1.35 1.28 1.18 0.7 0.88 132 S132R 0.15

0.8 0.15 132 S132T

132 S132V 0.23 3.29 2.39 2.07 0.8 0.58 132 S132W 0.24 0.08 0.06

132 S132Y 0.21 0.07 0.40 0.08

133 A133C 0.98 0.87 1.06 0.79 1.1 0.84 133 A133D 0.91 0.90 0.79 0.81 1.0 0.62 133 A133E 1.07 0.93 0.96 0.84 1.0 0.99 133 A133F 0.83 0.95 0.65 0.93 0.9 1.11 133 A133G 0.78 0.95 0.95 0.92 1.0 1.12 133 A133H

133 A133I 0.95 0.88 0.88 0.84 1.0 1.49 133 A133K 1.11 0.75 0.65 0.72 1.1 1.02 133 A133L 0.93 0.78 0.83 0.88 1.0 1.15 133 A133M 0.95 0.99 0.71 0.85 1.0 1.00 133 A133N

133 A133P 1.10 1.21 0.74 0.83 1.2 0.94 133 A133Q 0.85 1.25 0.98 0.79 1.1 1.07 133 A133R 0.93 0.51 0.41 0.65 1.1 0.97 133 A133S 1.05 1.00 0.94 0.82 1.0 1.06 133 A133T 0.96 1.03 0.78 0.82 1.1 1.14 133 A133V 0.98 0.95 0.89 0.87 1.1 1.07 133 A133W 0.73 0.86 0.42 0.73 1.1 1.09 133 A133Y 0.84 0.71 0.75 0.65 1.1 1.12 134 A134C 0.78 0.83 1.13 0.80 1.0 0.82 134 A134D 0.19

0.68 0.35 1.1 0.12 134 A134E 0.23

0.34 0.23

134 A134F 0.26 0.99 0.97 0.88 0.9 0.86 134 A134G 0.63 1.14 0.59 0.93 1.2 0.74 134 A134H 0.12

1.1 0.28 134 A134I 0.26 1.60 1.22 1.29 0.9 0.93 134 A134K 0.16

4.71 1.2 0.33 134 A134L 0.19 1.85 2.41 1.75 1.1 0.61 134 A134M 0.21 1.40 1.20 1.29 1.1 0.53 134 A134N

134 A134P 0.78 1.06 0.86 0.95 1.0 1.25 134 A134Q 0.19 0.12 0.36 0.32 1.1 0.10 134 A134R 0.25

134 A134S 0.97 1.04 0.91 0.92 1.1 1.12 134 A134T 0.94 1.03 0.86 1.04 1.0 1.04 134 A134V 0.39 1.27 1.04 0.84 0.9 1.14 134 A134W 0.19

0.32 0.15 1.1 0.08 134 A134Y

135 L135A 0.23 1.24 0.90 1.12 1.0 0.07 135 L135D 0.46

135 L135E 0.43 1.19 1.03 0.88 1.1 0.82 135 L135I 0.34 1.41 0.97 1.06 0.7 0.16 135 L135K 0.35

135 L135M 1.03 1.01 1.19 0.96 1.1 0.59 135 L135N 0.34

135 L135P 0.37

135 L135R 0.37 0.06

135 L135T 0.19 3.36 2.29 2.06 0.6 0.06 135 L135V 0.34 2.12 1.12 1.33 0.6 0.19 135 L135W 0.27 2.14 1.96 1.47 0.8 0.23 135 L135Y 0.34 1.91 2.03 1.66

136 K136A 0.57 0.80 1.04 0.83 0.9 0.80 136 K136C 0.51 1.02 1.04 0.74 0.9 0.81 136 K136D 0.21 1.62 1.47 0.92 0.4 0.47 136 K136E 1.03 0.92 0.73 0.82 1.2 1.03 136 K136F 0.27 1.35 1.57 1.15 0.6 0.82 136 K136G 0.44 1.09 1.12 0.91 0.7 0.82 136 K136H 0.89 0.99 1.00 0.68 1.1 1.08 136 K136I 0.20 2.18 2.48 1.44 0.4 0.47 136 K136L 0.65 1.05 0.71 0.90 1.0 1.16 136 K136M 0.69 1.02 0.87 0.87 0.9 1.09 136 K136N 0.60 1.08 0.88 0.81 1.0 0.88 136 K136P 0.20 0.23 0.74 0.27

136 K136Q

136 K136R 0.82 1.02 0.82 0.69 1.1 1.01 136 K136S 0.39 1.08 0.87 0.92 0.7 0.80 136 K136T 0.16

9.54 0.5 0.37 136 K136V 0.21 2.18 2.41 1.96 0.5 0.83 136 K136W 0.44 1.03 0.93 0.80 0.6 0.91 136 K136Y 0.25 1.78 1.41 1.21 0.4 0.94 137 A137C 1.00 0.91 0.95 0.71 1.1 1.08 137 A137D 1.14 1.04 1.00 0.81 1.0 1.06 137 A137E 0.75 0.91 1.10 0.88 1.1 1.03 137 A137F 0.59 1.01 0.78 0.90 1.0 1.41 137 A137G 0.72 1.01 0.91 0.78 1.1 1.24 137 A137H 1.02 0.95 0.78 0.91 0.9 1.03 137 A137I

137 A137K 0.90 0.96 0.52 0.90 1.0 1.17 137 A137L 0.84 0.85 0.82 0.89 1.1 1.07 137 A137M 0.93 1.09 0.89 0.85 1.0 1.06 137 A137N 1.01 1.02 0.62 0.77 1.0 1.38 137 A137P 0.18 3.85 3.42 1.76 0.2 0.10 137 A137Q 1.05 1.05 0.60 0.92 1.0 1.18 137 A137R 0.65 0.65 0.49 0.70 1.0 1.17 137 A137S 0.98 0.91 0.92 1.08 0.9 1.11 137 A137T 0.96 0.94 0.77 0.96 1.0 1.07 137 A137V 0.62 1.27 0.85 1.06 0.8 1.23 137 A137W 0.69 0.81 0.55 0.62 0.9 1.50 137 A137Y 0.83 1.05 0.73 0.66 0.9 1.33 138 A138C 0.85 1.04 1.10 1.14 0.9 1.07 138 A138D 0.17 1.47 4.55 2.27 0.3 0.16 138 A138E 0.36 1.44 0.96 1.13 0.9 0.83 138 A138F 0.18 2.55 2.71 1.96 0.8 0.31 138 A138G 0.52 1.27 1.35 1.07 0.9 1.16 138 A138H 0.20 2.04 2.24 1.84 0.7 0.52 138 A138I 0.78 0.93 0.98 1.11 0.9 1.18 138 A138K 0.29

138 A138L 0.27 1.23 1.19 1.42 0.9 0.70 138 A138M 0.71 0.88 0.89 1.00 1.0 0.91 138 A138N 0.16

4.25 0.9 0.25 138 A138P 0.32

0.09

138 A138Q 0.17 11.86  16.19  4.99 0.9 0.75 138 A138R 0.40

0.07

138 A138S 0.86 1.05 0.99 1.02 0.7 1.22 138 A138T 0.51 1.17 1.27 1.18 0.9 1.07 138 A138V 0.76 1.08 1.11 1.05 0.9 1.12 138 A138W 0.18

0.40 0.11

138 A138Y 0.17 5.98 9.05 3.30 0.6 0.51 139 V139A 0.69 1.06 1.06 0.97 0.8 0.94 139 V139C 1.19 1.03 1.09 0.95 1.0 1.30 139 V139D 0.23

0.07

139 V139E 0.23

139 V139F

139 V139G 0.21 0.40 0.60 0.65 0.5 0.25 139 V139H 0.25 0.75 0.74 0.73 0.8 0.06 139 V139I 0.85 0.84 0.73 1.02 1.0 0.43 139 V139K

139 V139L 0.75 0.98 0.84 1.09 0.8 0.28 139 V139M 0.61 0.97 0.67 1.01 0.6 0.49 139 V139N 0.47 0.83 0.76 1.14 0.9 1.20 139 V139P 0.39

139 V139Q 0.17

0.83 0.15

139 V139R 0.37

139 V139S 0.49 0.78 1.11 1.11 0.9 0.98 139 V139T 0.42 1.27 0.83 1.19 1.0 0.63 139 V139W 0.36

139 V139Y 0.31 0.17 0.26 0.25

140 D140A 0.45 0.70 0.72 0.81 0.2 0.61 140 D140C 0.56 0.90 1.02 0.89 0.8 0.88 140 D140E 1.02 1.20 0.98 0.92 0.9 1.01 140 D140F

140 D140G 0.52 0.80 0.79 0.85 0.7 0.86 140 D140H 0.50 0.47 0.53 0.67 0.7 0.72 140 D140I

140 D140K 0.48 0.25 0.53 0.47 0.8 0.85 140 D140L 0.42 0.54 0.78 0.84 0.1 0.97 140 D140M 0.48 0.77 0.81 0.82 0.3 0.95 140 D140N 0.88 0.86 0.84 0.83 0.9 0.97 140 D140P 0.30 0.06 0.09

140 D140Q 0.61 0.87 0.80 0.96 0.7 1.31 140 D140R 0.41 0.22 0.28 0.50 0.7 0.98 140 D140S 0.55 0.81 0.77 0.92 0.4 0.83 140 D140T 0.60 0.85 0.80 0.89 0.5 0.87 140 D140V 0.42 0.98 1.00 0.96 0.2 1.07 140 D140W 0.23 0.74 0.78 0.85 0.4 0.95 140 D140Y 0.50 0.79 0.74 0.83 0.6 1.05 141 K141A 0.87 0.87 1.11 0.93 1.0 1.06 141 K141C 0.78 0.73 1.11 1.04 1.0 1.11 141 K141D 0.82 0.95 1.23 1.04 1.0 1.14 141 K141E 1.18 0.80 1.10 1.00 1.0 0.97 141 K141F 0.70 0.84 1.27 1.04 1.0 1.13 141 K141G 0.94 0.84 1.15 1.07 1.1 1.09 141 K141H 1.00 1.03 1.09 1.04 1.2 1.08 141 K141I 0.60 0.94 1.23 1.00 1.1 1.25 141 K141L 0.66 0.87 1.29 1.01 1.1 1.14 141 K141M 0.79 1.00 1.17 1.02 1.0 1.24 141 K141N 1.05 0.90 1.30 1.03 1.1 1.17 141 K141P 0.28

0.09

141 K141Q 1.06 0.96 1.26 1.09 1.1 1.10 141 K141R 1.09 0.87 1.13 1.07 1.0 0.97 141 K141S 0.95 0.96 1.06 1.22 1.0 1.15 141 K141T

141 K141V 0.60 1.20 1.28 1.02 1.0 1.36 141 K141W 0.70 1.14 1.32 1.18 1.2 1.27 141 K141Y 0.91 1.16 1.07 1.06 1.1 1.16 142 A142C 0.79 1.03 0.92 0.89 1.1 1.17 142 A142D 0.35

142 A142E 0.34

142 A142F 0.28

142 A142G 0.46 1.32 1.20 0.96 1.0 1.18 142 A142H 0.25

0.10 0.06

142 A142I 0.25 1.60 1.39 1.46 0.6 0.81 142 A142K 0.37

142 A142L 0.29 1.24 1.40 1.19 0.6 0.70 142 A142M 0.22 1.21 1.62 1.31 0.6 0.38 142 A142N 0.31

142 A142P 0.29

142 A142Q 0.31

142 A142R 0.36

142 A142S 0.68 1.01 0.98 1.23 1.0 1.18 142 A142T 0.31 1.32 1.55 1.46 0.8 1.11 142 A142V 0.37 1.49 1.19 1.23 0.8 1.12 142 A142W 0.32

142 A142Y 0.29

143 V143A 1.05 0.81 1.04 0.90 0.9 0.88 143 V143C 0.87 1.00 1.14 0.89 1.0 1.08 143 V143D 0.95 0.95 1.03 0.97 1.0 1.05 143 V143E 1.12 0.87 1.05 1.02 1.0 1.08 143 V143F 0.88 0.76 1.00 0.81 0.9 0.81 143 V143G 0.71 0.90 1.16 1.15 0.9 1.11 143 V143H

143 V143I

143 V143K 0.84 0.61 0.72 0.96 1.1 1.00 143 V143L 0.78 0.78 1.13 0.83 0.9 1.11 143 V143M 0.83 0.94 1.05 1.11 0.9 0.99 143 V143N 0.91 0.90 1.00 1.20 1.0 1.13 143 V143P 0.20

5.50 0.7 0.12 143 V143Q 0.88 0.82 1.11 1.04 1.1 1.04 143 V143R 0.77 0.64 0.70 0.92 1.0 0.94 143 V143S 1.03 0.94 0.97 0.93 1.0 1.02 143 V143T 0.83 0.90 0.93 0.99 1.0 1.17 143 V143W 0.65 1.36 0.84 1.02 0.9 0.88 143 V143Y 0.21

0.51 0.21

144 A144C 1.17 0.98 0.85 0.88 1.0 1.02 144 A144D 1.29 1.18 1.11 0.99 1.0 0.96 144 A144E 1.17 1.08 0.76 1.00 1.0 1.13 144 A144F 0.96 1.20 0.73 0.94 1.0 1.16 144 A144G 1.09 1.08 0.98 1.02 1.0 0.99 144 A144H

144 A144I 0.97 1.29 0.79 0.97 1.1 1.06 144 A144K 1.28 1.00 0.57 0.77 1.1 0.90 144 A144L 1.11 1.18 0.79 1.08 1.0 1.03 144 A144M 1.06 1.08 0.84 1.07 1.0 1.05 144 A144N

144 A144P 0.18 1.75 2.60 1.24 0.4 0.30 144 A144Q 0.25

0.07

144 A144R 1.23 0.96 0.45 0.90 1.1 1.00 144 A144S 1.04 1.24 0.93 0.85 1.0 1.05 144 A144T 1.08 1.16 0.89 1.04 1.1 1.14 144 A144V 0.80 1.11 1.13 0.86 1.0 1.21 144 A144W 0.87 1.23 0.64 0.88 1.0 1.63 144 A144Y

145 S145A 1.09 0.97 1.13 0.94 1.0 0.99 145 S145C 1.10 0.72 1.03 1.00 1.1 1.03 145 S145D 1.24 1.03 1.06 1.08 1.1 1.01 145 S145E 1.24 0.90 1.20 0.90 1.1 0.95 145 S145F 0.84 0.81 1.15 1.12 1.1 1.22 145 S145G 1.06 0.77 1.13 1.06 1.0 1.11 145 S145H 1.21 0.93 1.04 1.05 1.1 1.02 145 S145I 0.79 0.42 1.24 1.03 1.1 1.24 145 S145K

145 S145L 0.87 1.02 1.25 1.08 1.1 1.13 145 S145M 1.00 0.86 1.06 1.04 1.0 1.08 145 S145N

145 S145P 0.34

0.07

145 S145Q 1.10 0.74 1.18 1.08 1.0 1.06 145 S145R 1.21 0.78 1.01 1.13 1.1 1.06 145 S145T 1.04 0.92 1.17 1.04 1.0 1.07 145 S145V 0.83 0.87 1.25 1.06 1.0 1.17 145 S145W 0.81 1.15 1.10 1.01 0.9 1.21 145 S145Y 0.48 0.88 1.28 1.13 0.9 1.29 146 G146A 0.48 1.04 1.18 1.08 1.0 1.02 146 G146C 0.50 1.01 1.15 0.98 1.1 0.97 146 G146D 1.08 0.86 1.02 1.00 1.1 1.07 146 G146E 0.82 0.79 1.12 0.98 1.0 1.04 146 G146F 0.50 0.88 1.03 1.06 1.0 1.02 146 G146H 0.92 0.86 1.17 1.06 0.9 1.09 146 G146I 0.16 0.37

0.53 0.9 0.07 146 G146K 0.89 0.72 1.09 0.98 0.9 1.07 146 G146L 0.18 2.22 3.81 1.88 1.1 0.59 146 G146M 0.34 1.18 1.21 1.22 1.0 1.09 146 G146N

146 G146P 0.18 0.49 0.60 0.25 0.2 0.08 146 G146Q 0.85 0.95 1.16 1.05 1.0 1.45 146 G146R 0.81 0.79 1.08 1.04 0.9 1.02 146 G146S 0.76 0.92 1.11 0.91 0.9 1.06 146 G146T 0.25 1.52 1.80 1.57 0.7 1.12 146 G146V 0.13

0.7 0.16 146 G146W 0.13

0.9 0.49 146 G146Y 0.21 1.66 2.23 1.62 0.9 0.88 147 V147A 1.13 1.04 1.09 0.92 1.1 0.90 147 V147C 0.87 1.19 1.25 0.99 1.1 0.90 147 V147D 0.21 2.29 3.05 2.09 1.2 0.53 147 V147E 0.53 0.98 1.17 0.93 1.0 1.12 147 V147G 0.64 1.25 1.42 1.04 1.0 0.93 147 V147H 0.70 1.23 1.30 0.94 1.2 0.93 147 V147I 0.98 1.25 0.94 0.94 1.1 1.04 147 V147L 0.70 1.16 1.29 1.15 1.0 0.97 147 V147M 0.97 1.00 1.07 0.90 1.0 1.14 147 V147P 0.31 1.71 2.12 1.52 0.8 1.13 147 V147Q 0.84 1.23 1.09 1.03 1.2 1.01 147 V147R 0.71 1.16 1.07 0.88 1.0 0.96 147 V147S 0.87 1.06 1.22 0.87 1.0 0.98 147 V147T 0.80 1.24 1.06 1.02 0.9 1.16 147 V147W 0.25 1.97 2.16 1.32 0.9 0.93 147 V147Y 0.26 2.34 2.31 1.50 0.9 0.78 148 V148A 0.56 1.06 0.76 1.03 0.8 0.74 148 V148D 0.29 0.07 0.29 0.21

148 V148E 0.21 0.62 0.99 0.67 0.9 0.14 148 V148F 0.73 0.96 1.18 1.06 0.9 0.85 148 V148G 0.23 0.70 1.12 0.98 0.9 0.26 148 V148H 0.30 1.07 1.68 1.39 0.8 0.74 148 V148I 0.70 0.98 1.20 1.02 1.1 0.91 148 V148K 0.31

0.09

148 V148L 0.98 1.05 1.11 1.07 1.1 0.80 148 V148M 0.64 0.94 1.06 1.01 0.8 0.74 148 V148N 0.41 1.38 1.35 1.11 0.8 1.11 148 V148P 0.27 0.61 0.87 0.76 1.0 0.21 148 V148Q 0.25 1.08 1.73 1.58 1.0 0.82 148 V148R 0.47

148 V148S 0.52 1.09 1.20 1.10 1.0 0.90 148 V148T 0.55 1.05 1.41 1.13 1.0 0.99 148 V148Y 0.22 1.60 1.45 1.60 0.6 0.37 149 V149A 0.80 0.96 1.10 0.99 1.0 0.99 149 V149C 0.86 1.11 0.96 0.99 1.2 0.89 149 V149D 0.22 0.83 1.23 1.11 1.3 0.32 149 V149E 0.18 2.65 3.71 2.50 1.0 0.40 149 V149F 0.92 1.15 1.31 1.07 1.0 0.23 149 V149G 0.24 0.90 0.72 1.05 1.0 0.28 149 V149H 0.25 0.54 0.75 0.70 1.2 0.26 149 V149I 0.84 0.96 1.08 0.85 1.1 0.80 149 V149L 0.69 1.02 1.11 1.11 1.1 0.98 149 V149M 0.82 1.09 1.11 1.07 1.1 0.82 149 V149P 0.46 0.94 1.23 1.04 1.2 1.25 149 V149R 0.50

149 V149S 0.37 1.12 1.42 1.31 1.1 1.18 149 V149T 0.66 0.88 1.16 1.09 1.1 1.11 149 V149W 0.25 0.44 0.50 0.59 1.3 0.12 149 V149Y 0.33 1.18 1.52 1.33 1.0 0.18 150 V150A 0.54 0.85 1.21 1.04 0.9 0.67 150 V150C 0.80 0.86 1.07 1.06 1.0 0.80 150 V150E 0.45

0.06

150 V150F 0.47 0.89 1.07 1.07 0.8 0.86 150 V150G 0.30

0.15 0.18

150 V150H 0.37

150 V150I 0.83 1.14 1.05 1.07 1.0 1.15 150 V150K 0.31 0.11

0.06

150 V150L 0.75 0.97 0.96 1.02 0.9 0.95 150 V150M 0.39 0.97 1.26 1.27 0.9 0.77 150 V150N 0.28 0.27 0.26 0.21 1.1 0.06 150 V150P 0.43

150 V150Q 0.31 1.25 1.67 1.46 1.0 1.05 150 V150R 0.48

150 V150S 0.33 1.08 1.22 1.17 0.8 0.52 150 V150T 0.61 0.71 1.28 1.09 1.0 0.72 150 V150W 0.43 0.06

150 V150Y 0.32

151 A151C 0.74 1.20 0.94 0.98 0.9 0.91 151 A151D 0.50

0.11

151 A151E 0.47

151 A151F 0.51

151 A151G 0.49 0.85 1.24 1.16 0.8 0.74 151 A151I 0.21 0.25 0.54 0.19

151 A151K 0.49

151 A151L 0.47

151 A151M 0.24 1.15 1.42 1.13 1.0 0.32 151 A151N 0.21 0.93 1.88 1.11 0.7 0.13 151 A151P 0.47

151 A151Q 0.35 0.20 0.20 0.21

151 A151R 0.48

151 A151S 0.79 0.96 1.26 1.08 1.0 0.51 151 A151T 0.46 1.36 1.20 1.18 0.6 0.56 151 A151V 0.38 0.95 1.08 1.45 0.6 0.61 151 A151W 0.56

152 A152C 1.40 0.76 0.77 0.94

152 A152E 1.63

152 A152F 0.38

152 A152H 0.46

152 A152K 0.64

152 A152L 0.46

152 A152M 1.47

152 A152N 0.67 0.11

0.14

152 A152P 2.05 0.91 0.91 0.95

152 A152Q 1.99

152 A152S 1.11 0.74 1.00 0.85 0.9 0.32 152 A152T 0.75 0.80 0.81 1.05

152 A152V 0.44 1.24 1.09 1.35

152 A152W 0.37

152 A152Y 0.45

153 A153C 0.54 1.02 1.03 0.96 0.5 0.67 153 A153D 0.20

0.16 0.06

153 A153E 0.36

153 A153F 0.50

153 A153G 0.51 1.03 1.06 1.03 0.5 0.64 153 A153H 0.35

153 A153I 0.14 0.56

153 A153K 0.36

153 A153L 0.22

0.10

153 A153M

153 A153N 0.22

0.11

153 A153P 0.20

0.27 0.07

153 A153Q 0.20

0.24 0.22 0.3 0.08 153 A153R 0.31

153 A153S 0.65 1.05 1.03 1.04 0.6 0.62 153 A153T 0.17 4.36 4.31 3.03

0.29 153 A153V 0.28 1.34 1.24 1.39 0.3 0.88 153 A153W 0.36

0.10

153 A153Y 0.26

154 G154A 0.43

154 G154C

154 G154D 0.29 0.49 0.43 0.45

154 G154E 0.47

0.09 0.07

154 G154F 0.37

154 G154H 0.25 0.21 0.35 0.56

154 G154I 0.43

154 G154K 0.35

0.07

154 G154L 0.28 0.38 0.51 0.49

154 G154M 0.27 0.24 0.66 0.49

154 G154N 0.21 0.55 0.54 0.59

154 G154P 0.37

154 G154Q 0.25 0.34 0.38 0.56

154 G154R 0.24

0.10

154 G154S 0.22 0.58 0.78 0.76 0.2 0.06 154 G154T 0.26 0.48 0.65 0.93

154 G154V 0.28

0.07 0.18

154 G154W 0.28

0.11

154 G154Y

155 N155A 1.36 0.08

0.13

155 N155C 0.94

0.06

155 N155D 2.13

155 N155F 0.86 0.07

0.13

155 N155G 1.90 0.25

0.49

155 N155H 1.16 0.14 0.09 0.22

155 N155I 0.64

155 N155K 0.73 0.09 0.08 0.18

155 N155L 0.61

0.08

155 N155M 0.75

155 N155Q 0.94

0.06

155 N155R 0.58 0.08 0.06 0.16

155 N155S 1.50 0.10 0.07 0.21

155 N155T 0.81

0.10

155 N155V 0.69

155 N155W 0.70

0.11

155 N155Y 1.10 0.11

0.17

156 E156A 1.12 0.69 0.60 0.84 1.0 0.87 156 E156C 1.10 0.61 0.70 0.83 1.0 0.85 156 E156F 1.11 0.41 0.57 0.89 1.0 1.12 156 E156I 0.43 0.59 0.64 0.86 0.5 0.86 156 E156K 0.99 0.42 0.41 0.78 0.5 1.30 156 E156L 0.82 0.55 0.60 0.83 0.8 1.31 156 E156M 1.10 0.46 0.57 0.86 0.9 1.31 156 E156N 1.17 0.38 0.48 0.72 1.0 0.91 156 E156P 0.26

0.16

156 E156Q 0.93 0.51 0.51 0.75 0.9 0.94 156 E156R 1.10 0.23 0.41 0.66 0.4 1.35 156 E156S 0.93 0.62 0.52 0.91 0.8 1.01 156 E156T 0.72 0.73 0.65 1.00 0.7 1.44 156 E156V 0.54 0.60 0.60 0.98 0.6 1.13 156 E156W 0.79 0.24 0.21 0.60 0.7 0.79 156 E156Y 1.10 0.35 0.43 0.72 0.9 1.09 157 G157A 0.48 0.83 0.87 0.92 0.6 0.62 157 G157C 0.60 0.63 0.79 0.95 0.4 0.18 157 G157D 0.49 0.68 0.87 0.79 0.4 0.20 157 G157E 0.58 0.62 0.82 0.69 0.2 0.12 157 G157F 0.34 0.38 0.60 0.68 0.2 0.19 157 G157H

157 G157I 0.34 0.34 0.53 0.54 0.1 0.06 157 G157K 0.33 0.33 0.68 0.62

0.21 157 G157L 0.40 0.33 0.54 0.60 0.1 0.06 157 G157M 0.43 0.58 0.72 0.66 0.2 0.11 157 G157N

157 G157P 0.45 0.32 0.42 0.58 0.1 0.09 157 G157Q 0.41 0.55 0.80 0.71 0.2 0.13 157 G157R 0.31 0.28 0.52 0.43 0.1 0.15 157 G157S 0.53 1.03 0.96 0.88 0.8 0.72 157 G157T 0.37 0.51 0.81 0.97 0.2 0.12 157 G157V 0.33 0.43 0.74 0.63 0.1 0.09 157 G157W 0.40 0.59 0.70 0.88 0.2 0.18 157 G157Y 0.29 0.74 0.80 0.80 0.3 0.27 158 T158A 0.94 0.98 0.98 0.92 0.8 1.10 158 T158C

158 T158D 0.68 1.09 1.09 1.04 1.1 0.94 158 T158E 1.10 1.09 1.03 0.98 1.2 0.95 158 T158F

158 T158G 0.77 1.11 0.47 1.06 0.8 0.75 158 T158H 0.85 1.04 0.95 0.92 0.9 0.87 158 T158I 1.02 1.08 0.75 0.91 1.0 0.96 158 T158K 0.83 1.05 0.53 0.85 0.8 0.97 158 T158L 0.71 1.06 0.65 0.83 0.8 0.73 158 T158M 0.80 0.97 0.71 0.97 0.7 0.71 158 T158N 0.79 1.16 0.69 0.85 1.0 0.80 158 T158P 0.58 1.12 0.88 0.86 0.7 0.66 158 T158Q 0.82 1.04 0.89 0.81 1.0 0.81 158 T158R 0.56 0.84 0.54 0.83 0.5 1.02 158 T158S 1.31 1.09 1.04 0.93 0.9 0.94 158 T158V 0.93 1.20 0.83 0.86 0.9 0.95 158 T158W 0.61 1.01 0.75 0.89 0.6 0.82 158 T158Y 0.75 1.01 0.53 1.04 0.7 0.84 159 S159A 0.92 0.93 0.90 1.07 0.7 0.78 159 S159C 1.16 1.08 1.18 0.87 1.1 0.93 159 S159D 1.41 1.26 1.15 1.05 1.1 0.92 159 S159E 1.07 1.04 1.13 1.07 1.0 0.90 159 S159F 0.73 1.14 0.93 1.06 0.4 0.74 159 S159G 0.88 1.14 1.13 0.91 0.6 0.86 159 S159H 1.10 0.95 0.85 0.88 1.0 1.05 159 S159I 0.90 1.03 1.02 0.92 0.4 0.63 159 S159K 1.24 1.37 0.92 1.00 1.0 1.08 159 S159L 0.77 1.09 1.15 1.25 0.4 0.77 159 S159M 0.81 1.02 1.22 0.92 0.5 0.70 159 S159N

159 S159P 0.72 1.20 0.94 1.05 0.3 0.62 159 S159Q 1.10 1.06 1.16 1.11 1.1 1.08 159 S159R 1.09 0.78 0.87 0.93 0.9 1.07 159 S159T 0.65 1.02 1.05 1.03 0.8 0.96 159 S159V 0.70 1.14 1.14 1.05 0.5 0.66 159 S159W 0.43 0.93 1.04 1.06 0.2 0.54 159 S159Y 0.37 1.07 1.11 1.27 0.5 0.90 160 G160A 0.51 0.83 0.96 0.81 0.6 0.63 160 G160C 0.85 0.75 1.06 0.83 0.9 0.86 160 G160D 1.17 0.71 1.28 0.88 1.0 0.90 160 G160E 1.05 0.85 1.31 0.92 1.0 0.92 160 G160F

160 G160H

160 G160I

160 G160K 0.79 0.75 0.79 0.88 0.4 0.89 160 G160L 0.36 0.92 1.00 1.00 0.5 0.52 160 G160M 0.41 0.70 0.86 0.87 0.4 0.46 160 G160N 0.92 1.05 1.21 0.93 0.9 1.00 160 G160P 0.51 0.82 1.15 0.69 0.7 0.63 160 G160Q 0.75 0.72 1.15 0.92 0.8 0.83 160 G160R 0.54 0.69 0.83 0.87 0.3 0.78 160 G160S 0.80 0.82 1.12 0.89 0.7 0.84 160 G160T 0.71 0.70 1.21 1.08 0.6 0.93 160 G160V 0.48 1.12 1.25 0.88 0.5 0.60 160 G160W 0.37 0.93 0.90 0.99 0.3 0.61 160 G160Y 0.46 0.90 1.11 1.06 0.4 0.61 161 S161A 1.08 1.15 1.21 0.95 0.8 1.00 161 S161C 1.31 0.93 1.12 0.82 1.2 1.04 161 S161D

161 S161E 1.35 1.12 1.21 1.00 1.2 0.92 161 S161F 0.58 0.96 1.18 1.02 0.9 1.17 161 S161G 1.37 1.13 1.14 0.96 1.1 0.93 161 S161H

161 S161I 1.01 1.18 1.10 0.94 0.9 0.86 161 S161K 0.97 0.88 1.00 1.02 0.9 1.04 161 S161L 1.12 1.25 0.96 0.87 1.0 0.96 161 S161M 1.07 1.08 1.03 0.99 1.0 0.95 161 S161N

161 S161P 1.30 1.26 1.19 1.07 1.0 1.04 161 S161Q 1.10 1.16 1.13 0.98 1.1 1.15 161 S161R 0.84 0.94 0.84 0.88 0.8 1.16 161 S161T 1.13 1.09 1.21 1.00 1.0 1.41 161 S161V 0.93 1.29 1.07 1.05 0.9 1.10 161 S161W 0.43 0.96 1.12 1.05 0.7 0.83 161 S161Y 0.70 1.05 1.05 0.95 0.8 0.99 162 S162A 0.75 1.09 1.00 0.96 1.0 0.92 162 S162C 1.24 0.94 0.95 0.89 1.1 0.93 162 S162D

162 S162E 1.41 1.16 0.93 0.89 1.1 0.99 162 S162F 0.45 0.94 0.96 0.82 0.9 0.77 162 S162G 0.76 1.16 0.94 0.91 1.0 1.03 162 S162H 1.29 0.95 0.71 1.02 1.0 1.02 162 S162I 0.53 1.06 0.84 0.89 1.0 0.98 162 S162K 1.38 1.05 0.81 0.94 1.0 1.09 162 S162L 0.66 1.25 0.55 0.91 1.0 0.84 162 S162M 0.73 1.09 0.64 1.03 0.9 1.00 162 S162N 1.39 0.89 0.87 1.00 1.1 1.09 162 S162P 0.56 1.06 0.87 0.89 0.7 0.66 162 S162Q 1.28 1.06 1.06 0.88 1.1 1.07 162 S162R 0.90 0.80 0.69 0.89 0.9 1.26 162 S162T 0.89 1.04 0.69 0.76 0.9 0.98 162 S162V 0.61 1.13 0.81 0.92 0.9 1.03 162 S162W 0.50 1.03 0.55 0.68 0.7 0.71 162 S162Y

163 S163A 0.32 0.71 0.78 0.89 0.2 0.30 163 S163C 0.35 0.88 0.55 0.85 0.2 0.26 163 S163D 0.56 0.92 0.90 0.86 0.1 0.45 163 S163E 0.38 0.93 0.84 0.83

0.33 163 S163F 0.29 0.77 0.70 0.68

0.25 163 S163G 1.10 1.02 0.86 0.93 0.6 0.85 163 S163H 0.25 0.97 0.70 0.98 0.1 0.29 163 S163I 0.31 0.73 0.72 0.93 0.1 0.20 163 S163K 0.28 0.73 0.79 0.81

0.30 163 S163L 0.34 0.76 0.53 0.79

0.36 163 S163M 0.33 0.71 0.71 0.76

0.28 163 S163N 0.34 0.81 0.91 0.71

0.30 163 S163P 0.99 1.05 0.78 0.95 0.4 0.63 163 S163Q

163 S163R 0.27 0.67 0.55 0.77 0.1 0.24 163 S163T 0.45 0.95 1.01 1.06 0.7 0.60 163 S163V 0.27 1.02 1.00 0.97

0.26 163 S163W 0.21 1.05 0.96 0.95 0.1 0.20 163 S163Y 0.31 0.81 0.66 0.63

0.36 164 T164A 0.38 0.40 0.53 0.76 0.1 0.21 164 T164C 0.29 0.51 0.70 0.74 0.1 0.11 164 T164D 0.51 0.82 0.98 0.98

0.18 164 T164E 0.39 0.79 1.27 1.14 0.8 0.43 164 T164F 0.27 0.33 0.34 0.72

0.15 164 T164G 0.40 0.51 0.76 0.70 0.1 0.26 164 T164I 0.19 0.44 0.67 0.86 0.3 0.07 164 T164K 0.28 0.41 0.64 0.74

0.29 164 T164L 0.22 0.90 1.06 1.33 0.1 0.18 164 T164M 0.30 0.40 0.66 0.81 0.4 0.19 164 T164N 0.36 0.71 0.78 0.92 0.4 0.51 164 T164Q 0.24 0.63 1.02 1.06

0.26 164 T164R 0.30 0.45 0.58 0.70

0.30 164 T164S 0.32 0.80 0.98 0.87 0.4 0.45 164 T164V 0.26 0.55 0.80 0.88 0.1 0.19 164 T164W 0.18 1.58 2.34 1.67 0.1 0.20 164 T164Y 0.20 1.10 1.76 1.62 0.1 0.19 165 V165A 0.19

0.28

165 V165C 0.22 0.53 0.65 0.92 0.4 0.23 165 V165E 0.24

0.08

165 V165F 0.22

0.11 0.12

165 V165H 0.15

0.2 0.16 165 V165I 0.37 0.89 1.17 1.15 1.1 0.87 165 V165K 0.28

165 V165L 0.28 0.62 0.66 1.12 0.8 0.54 165 V165M 0.30 0.61 0.84 1.10 0.7 0.53 165 V165P 0.46 0.87 0.80 0.84 0.8 0.70 165 V165Q 0.16

2.10

165 V165R 0.22

0.07

165 V165S 0.18

0.23

165 V165T 0.19 1.50 1.95 1.86 0.1 0.21 165 V165W 0.29

166 G166A 0.27 0.47 0.77 0.97 1.1 0.26 166 G166C 0.86 0.61 0.78 0.79 1.1 0.33 166 G166F 1.09 0.54 0.46 0.82 1.3 0.17 166 G166H 1.04 0.80 0.77 0.78 1.2 0.41 166 G166K 0.82 0.32 0.33 0.58 0.9 0.43 166 G166L 1.36 0.41 0.48 0.61 1.2 0.20 166 G166M 1.13 0.56 0.59 0.66 1.1 0.40 166 G166N 1.08 0.90 0.94 1.10 1.1 0.47 166 G166P 0.37 0.79 0.83 0.88 0.1 0.19 166 G166Q 1.21 0.66 0.81 0.96 1.1 0.57 166 G166R 0.87 0.41 0.43 0.88 0.9 0.55 166 G166S 1.09 0.80 1.04 0.75 1.0 0.26 166 G166T 1.16 0.68 0.65 0.77

166 G166V 1.01 0.44 0.85 0.75

166 G166W 1.10 0.65 0.95 0.99 1.1 0.06 166 G166Y 0.99 0.69 0.45 0.92 1.0 0.19 167 Y167A 0.68 1.35 1.13 1.28 0.7 0.57 167 Y167C 0.42 1.20 1.06 1.31 0.6 0.30 167 Y167D 0.27 1.36 1.64 1.29 0.1 0.07 167 Y167E 0.37 1.46 1.71 1.31 0.5 0.08 167 Y167F 1.01 0.96 1.11 0.99 0.9 0.83 167 Y167G 0.27 0.47 0.90 0.76

167 Y167H 0.33 0.93 1.06 1.15 0.5 0.47 167 Y167I 0.66 0.98 1.15 1.14 0.9 0.34 167 Y167K 0.16

1.11 0.23

167 Y167L 0.23 1.16 1.53 1.29 0.1 0.17 167 Y167M 0.23 1.69 1.28 1.35 0.4 0.22 167 Y167N

167 Y167P 0.25 1.80 1.86 1.64

167 Y167Q 0.18 1.16 1.36 1.60

167 Y167R 0.29

167 Y167S 0.30 1.37 1.27 1.32 0.2 0.30 167 Y167T 0.33 1.47 1.25 1.39 0.3 0.35 167 Y167V 0.60 0.96 1.06 1.07 0.8 0.44 167 Y167W 0.41 1.21 1.10 1.04 0.3 0.54 168 P168A 0.23 0.38 0.54 0.32

168 P168C 0.27 0.17 0.12

168 P168D 0.29 0.22 0.06

168 P168E

168 P168F 0.24 0.07

0.10

168 P168G 0.23

0.22

168 P168H 0.23 0.60 0.10

168 P168I 0.19

168 P168K 0.24 0.14 0.09

168 P168L 0.21 1.99 0.85 0.34

168 P168M 0.26 0.08 0.21

168 P168N

168 P168Q 0.24 0.06 0.11

168 P168R 0.23

0.20 0.09

168 P168S 0.25 0.30 0.12

168 P168T 0.21 2.95 0.29

168 P168V 0.18

168 P168W 0.22 0.27

0.07

168 P168Y 0.24

0.10

169 G169A 1.32 0.86 0.90 0.89 1.0 1.23 169 G169C 0.19 3.00 2.18 2.35 1.0 0.46 169 G169E 0.44 0.08

169 G169F 0.48

169 G169H 0.59

169 G169I 0.75

169 G169K 0.52

169 G169L 0.43

169 G169M 0.61

169 G169N 0.41

169 G169P 0.21 0.16

0.10

169 G169Q 0.30 0.20

0.11

169 G169R 0.49

169 G169S 0.38 1.02 0.83 1.03 0.9 0.63 169 G169T 0.23 0.15

0.09

169 G169V 0.49

169 G169W 0.42

169 G169Y 0.29 0.09

170 K170A 1.04 1.16 1.09 0.98 1.1 1.23 170 K170C 0.81 1.19 1.03 0.95 0.9 0.73 170 K170E 0.18 2.86 0.09 1.18

170 K170F 0.50 1.09 1.09 0.95 0.9 0.69 170 K170G 0.51 1.21 0.92 1.00 0.9 0.65 170 K170H 0.57 1.10 1.10 0.98 0.8 0.86 170 K170I 0.47 1.19 1.14 0.93 0.7 0.43 170 K170L 0.36 1.27 1.15 0.97 0.7 0.33 170 K170M 0.39 1.04 0.96 0.99 0.6 0.38 170 K170N 0.34 1.59 1.37 1.18 0.5 0.58 170 K170P 0.22 2.48 2.58 1.55 0.9 0.65 170 K170Q 0.51 1.32 1.22 1.05 0.8 0.63 170 K170R 1.13 1.12 1.08 1.05 1.1 1.14 170 K170S 0.51 1.30 1.13 0.90 0.9 0.75 170 K170T 0.29 1.48 1.50 1.06 0.5 0.48 170 K170V 0.62 1.13 1.17 1.08 0.8 0.78 170 K170W 0.30 1.08 1.13 0.97 0.8 0.48 170 K170Y 0.38 1.39 1.22 1.04 0.9 0.66 171 Y171A 0.22 0.15

0.15

171 Y171C 0.17 12.33 8.58 1.82 0.8 0.12 171 Y171D 0.17 4.55 3.45 1.13

171 Y171F 0.47 1.24 0.88 0.93 0.7 0.68 171 Y171G 0.43

171 Y171H 0.16

9.98 0.1 0.25 171 Y171I 0.20 0.18

171 Y171K 0.57 0.06

171 Y171L 0.18 4.11 3.35 2.44 0.3 0.25 171 Y171M 0.16

0.18 7.20

171 Y171N 0.17 2.21

0.47

171 Y171P 0.45

171 Y171Q 0.23 0.32

0.17

171 Y171R 0.49

171 Y171S 0.20

0.06

171 Y171T 0.18 0.37

171 Y171V 0.11

171 Y171W 0.49 1.37 1.02 1.02 0.6 0.40 172 P172A 0.83 1.13 1.08 1.09 1.0 1.14 172 P172C 0.69 1.22 1.17 0.77 0.9 1.06 172 P172E 0.80 1.30 1.16 1.01 1.2 1.01 172 P172F 0.40 1.25 0.99 1.14 0.8 0.92 172 P172G 0.34 1.36 1.22 1.23 1.0 0.87 172 P172H 0.52 1.09 0.91 1.08 0.9 1.03 172 P172I 0.46 1.38 1.11 1.11 0.9 1.07 172 P172K 0.66 0.99 0.61 0.90 1.0 1.05 172 P172L 0.52 1.50 1.08 1.14 1.0 1.02 172 P172M 0.55 1.23 1.14 1.08 1.0 1.02 172 P172N 0.67 1.09 0.96 1.01 0.9 1.05 172 P172Q 0.75 1.17 1.02 0.90 1.0 1.19 172 P172R 0.52 0.84 0.51 0.80 1.0 0.99 172 P172S 0.64 1.17 1.02 1.20 1.0 1.06 172 P172T 0.58 1.27 1.04 1.15 0.8 1.24 172 P172V 0.54 1.37 1.18 1.24 0.8 1.15 172 P172Y 0.29 1.67 1.29 1.41 0.8 0.88 173 S173A 0.89 1.16 0.72 1.02 0.9 0.93 173 S173C 0.81 1.19 0.89 1.05 0.9 0.98 173 S173D

173 S173E 0.96 0.90 0.78 0.98 1.0 0.95 173 S173F 0.51 1.07 1.17 0.87 0.6 0.82 173 S173G 0.64 0.93 0.65 0.91 0.8 0.59 173 S173H 0.49 1.35 0.88 1.18 0.8 0.92 173 S173I 0.44 1.16 1.05 1.30 0.8 1.10 173 S173K 0.70 0.66 0.57 1.03 0.7 0.95 173 S173L 0.56 1.10 1.02 1.35 0.9 0.84 173 S173M 0.69 1.11 1.16 1.00 0.8 1.01 173 S173N

173 S173P 0.45 1.14 1.02 1.22 0.9 0.89 173 S173Q 0.67 1.28 0.84 1.21 0.9 1.03 173 S173R 0.45 0.98 0.65 1.14 0.6 0.93 173 S173T 0.82 1.08 0.81 1.15 1.0 1.00 173 S173V 0.79 1.09 0.79 1.10 1.0 1.09 173 S173W 0.33 1.89 1.29 1.50 0.6 0.90 173 S173Y 0.39 1.71 1.01 1.38 0.7 0.87 174 V174A 0.45 1.44 1.21 1.10 0.8 1.00 174 V174C 0.80 1.14 1.08 1.21 0.9 1.19 174 V174D 0.20

0.65

174 V174E 0.22 0.36

0.08

174 V174F 0.22 0.58 0.18 0.16

174 V174G 0.19

0.2 0.13 174 V174H 0.23 0.50 0.12

174 V174I 0.37 1.48 0.86 1.14 0.6 0.58 174 V174K 0.22 0.49

0.08

174 V174L 0.21 92.96  66.79  4.24 0.5 0.34 174 V174M 0.20

2.70 0.1 0.15 174 V174N 0.17

0.2 0.13 174 V174P 0.20

14.42  0.2 0.40 174 V174Q

174 V174R 0.25 0.16

174 V174S 0.41 1.38 1.04 1.21 0.9 0.82 174 V174T 0.78 1.29 0.82 1.13 0.9 1.11 174 V174W 0.24

174 V174Y 0.24 0.12

175 I175A 0.21 6.10 9.32 1.84 0.4 0.31 175 I175C 0.61 1.10 1.06 1.16 0.9 0.92 175 I175D 0.23

0.23 0.06

175 I175E 0.19

0.4 0.18 175 I175F 0.32 1.69 1.23 1.30 0.6 0.81 175 I175G 0.25 0.39 0.13

175 I175H

175 I175K 0.24 0.18

175 I175L 0.90 1.27 0.89 1.04 0.8 1.10 175 I175M 0.92 1.17 0.82 1.05 1.0 0.98 175 I175N 0.22 0.16

0.15

175 I175P 0.23 0.09 0.06

175 I175Q 0.19

0.7 0.46 175 I175R 0.22 1.47

0.11

175 I175S 0.17

0.5 0.09 175 I175T 0.31 1.96 1.59 1.44 0.5 0.93 175 I175V 0.33 1.96 1.32 1.36 0.9 1.06 175 I175W 0.16

0.1 0.28 175 I175Y

176 A176C 1.04 0.99 0.79 1.00 1.1 1.15 176 A176D

176 A176E 0.31

176 A176F 0.34

176 A176G 0.24 0.55 0.86 1.10 0.5 0.37 176 A176H 0.34

176 A176I

176 A176K 0.38

176 A176L 0.28

0.07 0.10

176 A176M 0.57

176 A176N 0.19

0.41 0.53

176 A176P 0.36

176 A176Q 0.29

176 A176R 0.33

176 A176S 0.78 0.89 1.00 1.12 1.0 0.71 176 A176T 0.58 1.19 1.12 1.24 1.1 0.77 176 A176V 0.16 1.53

0.61

176 A176W 0.38

176 A176Y 0.34

177 V177A 0.67 0.50 0.83 0.93 0.4 0.82 177 V177C 0.49 0.77 0.95 1.10 0.7 0.83 177 V177D 0.51

177 V177E 0.49

177 V177F 0.52

177 V177G 0.34

0.06

177 V177H 0.46

177 V177I 0.37 0.89 1.25 1.25 0.5 0.89 177 V177K 0.39

177 V177L 0.42

177 V177M 0.48

177 V177N 0.46

177 V177P 0.43

0.07

177 V177Q 0.45

177 V177R 0.41

177 V177S 0.34 0.87 0.97 1.16 0.1 0.72 177 V177T 0.56 0.75 0.73 1.09 0.8 1.00 177 V177W 0.18 3.77 5.40 4.51 0.2 0.53 177 V177Y 0.40

178 G178C 0.26 0.06

178 G178D 0.48

178 G178E 0.49

178 G178F 0.46

178 G178H 0.47

178 G178I 0.50

178 G178K 0.68

178 G178L 0.48

178 G178M 0.51

178 G178N 0.47

178 G178P

178 G178Q 0.21 0.89 1.34 1.25

0.36 178 G178R 0.44

178 G178S 0.31 0.68 0.85 1.28

0.58 178 G178T 0.38

178 G178V 0.40

178 G178Y 0.40

179 A179C

179 A179D 0.28

0.06

179 A179E 0.31

179 A179F 0.21

0.14 0.24

179 A179G 0.92 1.06 0.88 1.19 0.4 0.72 179 A179H 0.34

179 A179I 0.19

0.06 0.17

179 A179K 0.30

179 A179L 0.18

0.33

179 A179M 0.21 0.36 0.57 0.65 0.1 0.13 179 A179N 0.19 0.09 0.42 0.55

0.26 179 A179P 0.30

0.07

179 A179Q 0.27

0.07

179 A179R 0.37

179 A179S 0.63 1.04 0.74 1.16 0.4 0.74 179 A179T 0.22 0.60 0.59 1.21

0.35 179 A179V 0.23 0.64 1.06 1.00

0.40 179 A179W

179 A179Y 0.20 0.17 0.49 0.62

180 V180A 0.70 0.98 0.76 1.05 0.1 0.78 180 V180C 0.99 1.03 0.73 1.08 1.0 0.91 180 V180D

180 V180E

180 V180F 0.16 1.66

1.51

180 V180G 0.21 1.11 1.49 1.28

0.49 180 V180H 0.17 2.27 2.90 1.90 0.1 0.14 180 V180I

180 V180K 0.14 0.43 0.06

180 V180L 1.08 0.98 0.64 1.06 0.9 1.05 180 V180M 0.58 0.77 0.80 1.00

0.67 180 V180N 0.36 1.12 0.91 1.09

0.82 180 V180P 0.38

180 V180Q 0.17 4.63 4.63 2.08

0.30 180 V180R 0.29

180 V180S 0.90 0.96 0.94 1.04 0.3 1.01 180 V180T 1.07 0.93 0.87 1.01 0.9 1.13 180 V180W 0.11

180 V180Y 0.13 0.14 0.09

181 D181A

181 D181C 0.80 0.88 0.79 0.89 0.5 0.84 181 D181E 0.86 1.01 0.71 1.22 0.3 0.86 181 D181F

181 D181G 0.89 0.84 0.71 1.06

1.12 181 D181H 0.86 0.70 0.54 0.95

0.88 181 D181I 0.21 0.63 0.66 1.28

0.61 181 D181K 0.47 0.18 0.30 0.65

0.92 181 D181L 0.54 0.56 0.43 0.87

0.91 181 D181M 0.65 0.63 0.67 0.96

0.90 181 D181N 1.07 0.79 0.62 0.93 0.2 1.06 181 D181P 0.20

0.07

181 D181Q 0.55 0.71 0.60 0.89

0.84 181 D181R 0.34 0.06 0.22 0.53

0.77 181 D181S 0.88 0.73 0.73 1.02

1.07 181 D181T 0.93 0.78 0.63 0.85

0.98 181 D181V 0.20 0.81 1.44 1.58

0.53 181 D181W 0.41 0.38 0.50 0.74

0.89 181 D181Y 0.43 0.64 0.42 1.03

1.00 182 S182A 0.96 0.97 1.09 1.02 0.9 0.94 182 S182C 1.10 1.03 1.06 0.85 1.1 1.00 182 S182D 0.92 1.22 1.07 1.01 1.1 1.06 182 S182E

182 S182F 0.88 1.14 1.07 1.00 0.4 1.20 182 S182G 1.16 1.09 1.03 1.00 0.9 0.81 182 S182H 1.09 1.13 1.04 0.93 0.8 0.91 182 S182I 0.87 1.13 1.17 1.15 0.7 1.15 182 S182K 1.14 0.50 0.66 1.08

0.97 182 S182L 0.88 0.88 1.07 0.98 0.4 1.00 182 S182M 1.00 0.96 1.22 0.95 0.8 1.05 182 S182N

182 S182P 1.26 0.77 1.17 1.00 0.9 0.77 182 S182Q 0.94 1.28 1.04 0.98 1.0 1.08 182 S182R 1.08 0.69 0.57 1.02

1.18 182 S182T 0.95 0.82 1.19 0.92 0.8 0.98 182 S182V 0.79 1.02 1.31 1.07 0.8 1.19 182 S182W 0.32 1.48 1.36 1.36 0.3 1.04 182 S182Y 0.86 1.07 1.05 0.98 0.5 1.22 183 S183A 1.09 0.88 1.12 1.03 0.9 0.99 183 S183C 1.09 1.22 1.01 0.91 1.1 0.84 183 S183D

183 S183E 1.06 0.84 1.01 0.93 1.2 1.04 183 S183F 0.97 0.91 1.35 0.83 0.9 1.06 183 S183G 0.98 0.77 0.97 1.04 1.0 0.84 183 S183H 1.10 1.10 0.84 1.00 1.0 0.85 183 S183I 1.11 1.07 1.02 1.01 0.9 1.02 183 S183K 1.08 0.68 0.67 0.95 0.2 0.93 183 S183L 1.02 0.84 0.85 1.00 1.0 1.01 183 S183M 1.05 1.03 1.23 1.05 1.0 0.87 183 S183N 1.08 0.85 1.02 1.02 1.1 0.95 183 S183P 0.31 1.26 1.29 0.99

0.58 183 S183Q 0.99 0.66 1.23 0.98 1.1 0.95 183 S183R 1.06 0.67 0.70 0.95 0.1 0.93 183 S183T 0.92 1.20 1.25 1.02 1.0 1.12 183 S183V 0.90 1.20 1.10 0.93 1.0 1.11 183 S183W 0.71 1.03 1.00 1.06 0.7 1.26 183 S183Y 0.95 0.89 0.91 1.12 1.0 1.11 184 N184A 0.27 1.40 1.89 1.40 0.7 0.71 184 N184C 0.90 1.16 1.02 1.06 1.0 1.10 184 N184D 0.90 1.03 1.20 0.96 1.1 0.96 184 N184E 0.83 1.18 1.09 0.90 0.9 1.06 184 N184F 0.84 0.86 0.99 1.14 0.5 1.03 184 N184G 0.99 0.91 1.19 0.93 0.8 0.91 184 N184H 0.94 1.06 1.11 1.02 0.6 0.97 184 N184I 0.75 1.04 1.07 0.98 0.2 1.03 184 N184K 0.92 0.90 0.79 0.91

0.94 184 N184L 0.95 1.36 0.87 1.09 0.7 0.93 184 N184M 1.05 0.99 1.06 0.97 0.7 0.97 184 N184P 0.78 0.78 1.02 0.79 0.1 0.82 184 N184Q 0.82 0.78 1.10 1.10 0.6 1.05 184 N184R 0.93 0.69 0.89 0.93

0.93 184 N184S 0.88 1.02 0.97 1.06 0.7 1.04 184 N184T 0.80 1.16 1.14 0.90 0.4 1.19 184 N184V 0.72 1.30 1.07 1.02 0.3 1.02 184 N184W 0.80 0.92 1.28 0.99 0.4 1.26 184 N184Y 0.80 0.93 1.06 1.16 0.6 1.10 185 Q185A 1.01 0.84 1.15 1.06 0.9 1.08 185 Q185C 0.95 1.15 1.09 0.92 1.1 1.00 185 Q185D 0.29 2.02 1.65 1.42 0.6 0.56 185 Q185E 0.77 1.37 1.07 0.91 1.2 1.03 185 Q185F 0.84 1.05 1.09 0.94 0.6 1.14 185 Q185G 0.74 0.79 1.29 1.00 0.7 1.02 185 Q185H 1.00 0.88 0.91 1.02 0.9 1.09 185 Q185I 0.87 1.46 0.98 0.95 0.9 1.24 185 Q185K 0.98 0.68 0.73 0.85 0.7 0.97 185 Q185L 0.87 0.99 0.96 1.04 0.7 1.00 185 Q185M 0.93 0.91 1.09 1.05 1.0 1.01 185 Q185N 0.97 1.14 1.11 1.08 1.1 1.05 185 Q185P 0.17

185 Q185R 0.91 0.75 0.80 0.99 0.4 1.07 185 Q185S 0.83 1.38 1.04 1.06 0.8 1.06 185 Q185T 0.82 1.36 1.28 1.13 1.0 1.17 185 Q185V 0.94 1.04 1.30 0.99 0.8 1.16 185 Q185W 0.81 0.85 0.85 0.87 0.1 1.14 185 Q185Y 0.74 0.95 1.05 1.26 0.7 1.28 186 R186A 0.38 1.03 1.51 1.09 0.7 0.45 186 R186C 0.36 1.91 1.61 1.05 0.6 0.47 186 R186D 0.21 11.05  16.42  0.21

186 R186E 0.21 23.12  23.90  1.79 0.1 0.11 186 R186F 0.33 1.32 1.44 0.88 0.2 0.29 186 R186G 0.31 2.21 1.88 1.19 0.2 0.60 186 R186H 0.50 1.13 1.34 1.17 0.7 0.73 186 R186I 0.38 1.34 2.12 1.26 0.9 0.80 186 R186K 0.62 0.95 1.19 1.00 0.6 0.92 186 R186L 0.54 1.58 1.44 1.20 0.9 0.89 186 R186M

186 R186N 0.25 2.46 3.74 1.52 0.3 0.43 186 R186P 0.24 2.96 2.29 0.95 0.1 0.19 186 R186Q 0.37 1.48 2.05 1.32 0.8 0.85 186 R186S 0.27 2.44 1.91 1.39 0.3 0.40 186 R186T 0.22 8.56 6.97 2.69 0.4 0.36 186 R186V 0.42 2.00 2.04 1.42 0.9 0.75 186 R186W 0.63 1.54 1.71 1.12 1.1 0.98 186 R186Y 0.38 1.50 1.98 1.37 0.8 0.71 187 A187C 0.77 0.75 1.06 0.84 0.2 0.31 187 A187D 0.93 1.51 0.99 1.03 0.4 0.17 187 A187E 0.72 1.41 1.49 1.00 0.2 0.34 187 A187F 0.73 1.02 1.07 0.93 0.1 0.43 187 A187G 0.90 1.04 1.12 0.93 0.6 1.05 187 A187H

187 A187I 0.34 1.14 1.55 0.93

0.43 187 A187K 0.23 1.21 1.45 1.18

0.36 187 A187L 0.55 0.77 1.15 0.90

0.33 187 A187M 0.40 1.03 1.34 0.93

0.42 187 A187N 0.74 1.11 1.39 1.03 0.5 1.22 187 A187P 1.08 1.15 1.12 0.92 0.7 0.69 187 A187Q 0.48 1.32 1.24 0.92

0.41 187 A187R 0.24 0.48 0.81 0.70

0.29 187 A187S 0.68 1.14 1.13 1.06 0.4 0.94 187 A187T

187 A187V 0.46 1.14 1.14 0.91

0.60 187 A187W 0.93 0.95 0.99 1.07 0.7 0.41 187 A187Y 1.02 1.05 1.25 0.79 0.5 0.40 188 S188A 1.14 0.93 1.08 0.96 0.9 0.92 188 S188C 1.24 1.07 1.27 0.81 1.0 0.85 188 S188D 1.08 1.03 1.33 0.94 1.2 0.86 188 S188E 1.03 1.18 1.29 0.98 1.1 1.00 188 S188F 0.91 0.98 1.08 0.86 0.8 0.92 188 S188G 1.06 0.99 1.09 0.94 0.9 0.89 188 S188H 1.01 0.92 1.00 0.91 0.9 1.01 188 S188I 0.94 0.79 1.24 1.01 0.9 0.96 188 S188K 1.14 0.64 0.89 1.00 0.5 1.05 188 S188L 1.01 1.07 1.16 0.82 0.8 0.98 188 S188M 0.98 0.73 1.28 0.90 0.8 0.98 188 S188N

188 S188P 1.05 1.05 1.23 1.01 1.0 0.90 188 S188Q 0.97 1.01 1.17 1.00 0.9 1.03 188 S188R 0.48 0.91 1.28 1.13 0.5 1.00 188 S188T 0.82 0.95 1.37 1.01 0.9 1.08 188 S188V 0.84 0.97 1.25 0.96 0.8 1.15 188 S188W 0.80 0.63 1.04 0.70 0.8 0.81 188 S188Y 0.77 0.90 1.11 0.86 0.9 0.94 189 F189A 0.79 0.82 0.85 0.96

0.39 189 F189C 1.16 0.82 0.77 0.86 0.3 0.15 189 F189D 2.06 1.03 0.88 0.94 0.4 0.28 189 F189H 0.65 0.76 0.73 0.98

0.38 189 F189I 0.78 0.98 0.99 1.05

0.33 189 F189K 0.47 0.65 0.62 1.01

0.57 189 F189L 1.02 0.90 0.73 0.89

0.39 189 F189M 1.67 1.01 0.89 1.02 0.1 0.40 189 F189N 1.31 0.83 0.77 0.82 0.1 0.83 189 F189P 0.43 0.87 0.81 1.03

0.23 189 F189Q 0.80 0.68 0.75 0.78

0.38 189 F189R 0.60 0.61 0.52 0.98

0.51 189 F189S 0.93 0.91 1.08 1.06 0.1 0.81 189 F189T 0.74 1.01 1.10 0.99 0.1 0.92 189 F189V 0.70 1.07 0.83 0.93

0.36 189 F189W 0.59 0.57 0.71 0.81 1.0 0.54 189 F189Y 0.66 0.62 0.86 0.96 0.5 0.53 190 S190A 0.35 1.19 1.27 0.80 0.1 0.57 190 S190C 0.62 0.82 1.11 0.69 0.6 0.68 190 S190D 0.19

190 S190E 0.20

0.23

190 S190F 0.25 0.29

190 S190G 0.27 1.50 2.17 1.30 0.1 0.56 190 S190H 0.22

0.13

190 S190I 0.20 0.72 0.41 0.11

190 S190K 0.24 0.14

0.07

190 S190L 0.19 0.18

190 S190M 0.19

190 S190N 0.23 1.60 2.04 1.06 0.1 0.12 190 S190P 0.18 0.09

190 S190Q 0.18 0.08

190 S190R 0.22

0.65

190 S190T 0.31 1.03 1.36 1.15 0.3 0.49 190 S190V 0.17

0.32 190 S190W 0.25

190 S190Y

191 Q191A 0.93 0.67 1.11 0.98 0.9 0.66 191 Q191C 0.44 0.72 0.91 0.96 0.3 0.32 191 Q191D 0.24 0.14 0.24 0.10

191 Q191E 0.24 0.49 0.20 0.20

191 Q191F 0.25

191 Q191G 0.77 0.75 0.73 0.74 0.7 0.33 191 Q191H 0.20

0.46 1.53

191 Q191I 0.18

0.13

191 Q191K 0.17

191 Q191L 0.19

191 Q191M 0.20

0.15 0.41

191 Q191N 0.72 0.70 1.34 1.14 0.1 0.56 191 Q191P 1.19 0.60 0.59 0.62

191 Q191R 0.20

0.25 0.37

191 Q191S

191 Q191T 0.32 1.03 0.92 0.82 0.1 0.10 191 Q191V 0.33 0.98 0.62 0.74 0.1 0.09 191 Q191W 0.21

0.08

191 Q191Y 0.18

192 Y192A 0.86 0.94 1.08 0.97 0.8 1.08 192 Y192C

192 Y192D 0.24 1.91 2.19 1.17 0.1 0.11 192 Y192E 0.35 1.44 1.58 1.09

0.22 192 Y192F 0.51 0.70 0.98 0.87 0.4 0.55 192 Y192G 0.43 0.66 0.98 0.99 0.2 0.47 192 Y192H 0.45 0.85 0.66 0.82 0.2 0.49 192 Y192I

192 Y192K 0.34 0.53 1.15 0.70

0.24 192 Y192L 0.23 1.94 1.92 1.49

0.19 192 Y192M 0.41 0.90 0.93 0.84 0.1 0.39 192 Y192N 0.33 1.16 1.47 1.01 0.1 0.66 192 Y192P 0.34 0.88 0.38 0.60 0.1 0.13 192 Y192Q 0.36 2.14 1.27 1.17 0.2 0.56 192 Y192R 0.31 0.47 0.75 0.66

0.18 192 Y192S 0.63 0.82 1.15 0.93 0.7 0.88 192 Y192T 0.72 0.73 1.08 0.98 0.9 0.93 192 Y192V

192 Y192W 0.46 1.01 1.27 0.96

0.54 193 G193A 0.22 0.68

0.06

193 G193C 0.20 0.24

193 G193D 0.18

193 G193E 0.29

193 G193F 0.22

193 G193H 0.21 2.68

193 G193I 0.23

193 G193K 0.24 0.09 0.10

193 G193L 0.23 0.22

193 G193M

193 G193N 0.21

23.24 0.16

193 G193P 0.22 0.56 0.24 0.09

193 G193Q 0.21 2.43

0.09

193 G193R 0.19

193 G193S 0.20

0.84

193 G193T 0.22 4.84 0.51 0.10

193 G193V 0.21 2.28 1.17

193 G193W 0.21

0.27

193 G193Y 0.38

194 P194A 0.69 1.09 0.94 0.95 0.8 1.16 194 P194C 0.75 1.19 1.18 1.19 1.0 1.41 194 P194D

194 P194E 0.70 1.52 1.09 1.03 1.0 1.25 194 P194F

194 P194G 0.48 1.23 0.92 1.12 0.7 0.81 194 P194H 0.76 1.13 1.00 1.15 1.0 1.03 194 P194I 0.48 1.63 1.09 1.21 0.9 1.12 194 P194K 0.72 0.79 0.90 0.90 0.6 0.98 194 P194L 0.58 1.58 0.87 1.29 0.9 1.09 194 P194M 0.60 1.36 1.09 1.06 0.8 1.47 194 P194N 0.52 1.82 1.00 1.23 0.1 1.69 194 P194Q 0.60 1.24 1.02 1.16 0.8 1.09 194 P194R 0.18

194 P194S 0.69 1.19 0.94 1.13 0.8 1.10 194 P194T 0.58 1.32 1.37 1.10 0.9 1.21 194 P194V 0.48 1.67 1.08 1.18 0.8 1.36 194 P194W 0.57 1.27 1.17 1.10 0.9 1.16 194 P194Y

195 E195A 0.26 0.78 0.71 0.64 0.1 0.26 195 E195C 0.25 1.37 0.92 0.57 0.4 0.22 195 E195D 0.34 1.09 0.84 0.86 0.7 0.38 195 E195F 0.17

0.5 0.09 195 E195G 0.71 0.95 0.44 0.77 0.3 0.52 195 E195H 0.26 0.67 0.38 0.48 0.1 0.08 195 E195I 0.17

0.12

195 E195K 0.22 3.69 2.57 2.17 0.3 0.47 195 E195L 0.18

195 E195M 0.20

2.57 0.1 0.19 195 E195N

195 E195P 0.18

0.2 0.06 195 E195Q 0.30 1.29 0.69 1.02 0.2 0.69 195 E195R 0.18

195 E195S 0.25 1.14 0.72 0.80

0.30 195 E195T

195 E195V 0.16

195 E195W 0.22 4.29 1.26 1.32 0.1 0.10 195 E195Y

196 L196A 0.19

196 L196C 0.20

7.45 0.1 0.15 196 L196D 0.24 0.43 0.07 0.10

196 L196E

196 L196F 0.17

196 L196G 0.17

0.1 0.09 196 L196H 0.30 0.29

196 L196I 0.38 1.68 1.15 1.17 0.8 1.03 196 L196K 0.16

0.09

196 L196M 0.37 1.52 1.04 1.06 0.2 0.72 196 L196N 0.16

0.2 0.08 196 L196P 0.24 0.54

0.13

196 L196Q 0.16

196 L196R 0.16

196 L196S 0.15

0.09

196 L196T 0.24 3.86 2.91 2.68 1.0 0.69 196 L196V 0.34 1.95 1.28 1.45 0.7 0.79 196 L196W 0.19

2.7 0.09 196 L196Y 0.20

0.37

197 D197A 0.45 0.74 1.09 1.05 0.5 0.66 197 D197C 0.38 1.02 1.11 0.97 0.3 0.55 197 D197F 0.16 0.38 0.51 1.24

197 D197G 0.37 1.06 1.07 1.18 0.3 0.60 197 D197H 0.15

0.38

197 D197I 0.18 3.13 4.06 2.64

0.30 197 D197K 0.14

0.1 0.10 197 D197L 0.16

19.01  0.1 0.18 197 D197M 0.18 1.52 0.68 1.10 0.1 0.09 197 D197N 0.86 0.93 1.16 0.88 0.5 0.85 197 D197P 0.36

197 D197R 0.13

197 D197S 0.28 0.18 0.28 0.35 0.9 0.11 197 D197T 0.53 0.94 1.20 1.14 0.5 0.88 197 D197Y 0.24

198 V198A 0.58 0.88 0.86 1.11 0.2 0.96 198 V198C 0.84 0.78 1.11 1.00 0.8 0.94 198 V198D 0.20 1.23 1.82 1.45 1.1 0.34 198 V198E 0.22

0.06 0.10

198 V198F 0.76 0.78 0.72 1.00 0.9 0.76 198 V198H 0.20 0.57 1.01 0.96 0.2 0.18 198 V198I 0.83 0.41 0.94 0.98 1.0 0.87 198 V198K 0.29

198 V198L 0.90 0.67 0.73 0.94 1.0 1.13 198 V198M 0.75 0.78 1.03 1.08 0.8 0.96 198 V198N 0.23 0.08 0.09 0.26

198 V198P 0.45

198 V198Q 0.16

12.00  0.1 0.26 198 V198R 0.46

198 V198S 0.32

198 V198T 0.42 0.99 1.05 1.06 0.2 1.05 198 V198W 0.13

0.2 0.29 198 V198Y 0.53 0.67 1.19 1.12 0.8 1.00 199 M199A 0.49 1.04 0.94 1.10 0.1 0.79 199 M199C 0.64 0.88 0.85 0.80 0.7 0.66 199 M199D 0.16

0.88

199 M199E 0.17

8.86 0.21

199 M199F 0.17 28.65  28.81  2.58 0.1 0.23 199 M199G 0.18 1.09 0.55 0.93 0.1 0.12 199 M199H 0.19 0.52

0.41

199 M199I 0.43 1.20 1.02 1.04

0.75 199 M199K 0.34 0.07

199 M199L 0.34 1.28 0.88 1.05

0.51 199 M199N 0.20 0.90 0.97 0.93

0.22 199 M199P 0.50

199 M199Q 0.23 2.11 1.65 1.69 0.8 0.63 199 M199S 0.54 1.12 0.88 1.00 0.3 0.93 199 M199T 0.53 1.22 1.06 1.02 0.3 0.87 199 M199V 0.66 1.14 0.97 0.96 0.9 1.05 199 M199W 0.13

0.12

199 M199Y 0.13

0.09

200 A200C 0.70 1.32 0.86 1.16 0.6 1.17 200 A200D

200 A200E 0.32

200 A200F 0.18

200 A200G 0.83 1.19 1.05 1.08 0.6 1.08 200 A200H 0.21 4.98

0.16

200 A200I 0.26 0.23

0.09

200 A200K 0.25 0.12

200 A200L 0.18

1.0 0.06 200 A200M 0.18

200 A200N 0.47 1.33 1.20 1.17 0.7 1.28 200 A200P 0.23 0.61

0.07

200 A200Q

200 A200R 0.20

0.24

200 A200S 0.72 1.23 0.80 1.07 0.5 0.91 200 A200T 0.35 1.73 0.95 1.35 0.2 0.71 200 A200V 0.24 5.13 2.34 2.54

0.41 200 A200W 0.22 0.87 0.41 0.13

200 A200Y 0.21 2.63

0.10

201 P201A 0.65 0.61 0.87 1.08 0.9 0.79 201 P201C 0.47 1.07 0.95 1.30 0.2 1.06 201 P201D 0.15

201 P201E 0.29

201 P201F 0.44 1.13 0.94 1.21

1.02 201 P201G 0.54 0.42 1.08 1.21 0.6 0.91 201 P201H 0.40 0.65 1.21 1.15 0.1 0.90 201 P201I 0.18 1.05 0.64 1.28 0.1 0.12 201 P201K 0.16

10.07 

0.41 201 P201L 0.25 1.65 1.71 2.07

0.63 201 P201M 0.25 1.13 1.49 1.68

0.54 201 P201N 0.41 1.05 1.26 1.38 0.1 0.75 201 P201R 0.18 0.30

0.39 0.4 0.06 201 P201S 0.43 0.66 1.21 1.35 0.1 1.06 201 P201T 0.20 3.99 4.09 3.50

0.88 201 P201V 0.18 8.32 11.79  6.01

0.68 201 P201W 0.14

0.1 0.18 201 P201Y 0.58 0.73 0.91 1.11 0.7 1.17 202 G202A 0.33 0.40 0.49 0.61

0.44 202 G202C 0.39

202 G202D 0.35

0.08

202 G202E 0.41

202 G202F 0.38

202 G202H 0.38

0.07

202 G202I 0.40

202 G202K 0.37

202 G202L 0.37

202 G202M 0.33

0.06

202 G202N 0.36

202 G202P 0.37

202 G202Q 0.34

202 G202R 0.36

202 G202S 0.16

1.08

202 G202T 0.35

202 G202V 0.35

202 G202W 0.33

202 G202Y 0.36

203 V203A 0.51 1.07 1.26 1.24 0.3 1.48 203 V203C 0.93 1.10 1.10 0.83 1.0 0.66 203 V203D 0.54 1.12 1.62 1.23 1.1 1.09 203 V203E 0.57 0.88 1.05 1.13 1.1 0.88 203 V203F 0.46 1.06 1.28 1.11

1.00 203 V203G 0.17 8.72 7.71 4.86 0.1 0.33 203 V203H 0.59 0.87 0.81 0.89 0.1 0.30 203 V203I 0.81 0.63 1.05 0.93 0.8 0.77 203 V203K 0.62 0.60 0.73 0.87

1.10 203 V203M 0.77 0.98 1.14 1.00 0.6 0.99 203 V203N 0.47 1.05 1.38 1.22 0.1 0.99 203 V203P 0.23

203 V203Q 0.62 0.90 1.18 1.13 0.5 1.19 203 V203R 0.45 0.75 0.59 0.85

1.03 203 V203S 0.55 0.93 1.10 1.04 0.2 1.07 203 V203T 0.65 0.90 1.31 1.07 0.6 1.01 203 V203W 0.54 0.91 1.14 1.19

1.03 203 V203Y 0.43 0.94 1.21 1.05 0.1 0.97 204 S204A 0.97 0.86 1.00 0.81 1.2 1.06 204 S204C 0.90 1.00 1.05 0.89 1.4 0.85 204 S204F 0.86 0.39 0.60 0.82 0.7 1.06 204 S204G 0.88 1.01 1.19 0.75 1.1 1.50 204 S204H 0.68 0.72 0.81 0.95 1.0 1.21 204 S204I 0.66 0.79 0.99 0.83 0.7 0.91 204 S204K 0.90 0.74 0.64 0.87 0.1 0.93 204 S204L 0.77 0.85 0.82 0.93 0.9 0.90 204 S204M 0.90 0.75 1.10 0.95 0.8 0.90 204 S204P 0.22 0.06

0.12

204 S204Q 0.87 0.84 1.06 0.94 1.3 0.96 204 S204R 0.83 0.42 0.60 0.78

0.97 204 S204T 0.92 0.78 0.86 0.80 0.9 1.09 204 S204V 0.82 0.71 0.79 0.85 0.7 1.20 204 S204W 0.74 0.39 0.67 0.79 0.6 0.97 204 S204Y 0.75 0.52 1.04 0.87 0.7 1.03 205 I205A 0.40 0.78 0.92 0.93

0.61 205 I205C

205 I205D 0.27 0.35

205 I205E 0.23 0.46

205 I205F 0.27 0.27

205 I205G 0.19

0.15

0.1 0.11 205 I205H 0.20

4.55 0.2 0.08 205 I205K 0.20

0.99 0.30

205 I205L 0.30 1.37 1.00 0.86

0.53 205 I205M 0.20

4.69 0.1 0.26 205 I205N

205 I205P 0.23 0.79

205 I205Q 0.20

3.32

0.34 205 I205R 0.18

0.12

205 I205S 0.20

5.15

0.48 205 I205T 0.77 1.60 1.20 1.11 0.8 1.29 205 I205V 0.95 1.25 1.08 1.11 1.3 1.03 205 I205W 0.20

0.13

205 I205Y 0.19

206 Q206A 1.09 0.84 1.24 1.05 0.7 0.72 206 Q206C 1.10 1.13 1.03 1.12 1.4 0.94 206 Q206D 1.02 1.23 1.04 1.01 1.3 0.84 206 Q206E 1.01 1.26 1.14 1.16 1.4 0.97 206 Q206F 0.98 1.00 0.66 0.95

0.94 206 Q206G 1.03 0.91 0.66 1.03

0.72 206 Q206H 1.06 1.00 0.97 1.11 1.0 0.92 206 Q206I 1.12 1.00 0.99 1.04 0.5 0.87 206 Q206K 1.11 0.84 0.75 1.13 0.1 0.86 206 Q206L 1.03 0.89 0.93 0.94 0.7 1.02 206 Q206M 0.77 1.09 0.93 1.06 0.8 0.95 206 Q206N 1.03 1.07 1.08 1.06 1.1 0.91 206 Q206P 0.94 1.01 1.00 1.02 0.9 0.86 206 Q206R 1.05 0.78 0.52 0.98

1.03 206 Q206S 0.92 1.21 0.98 1.00 0.9 0.97 206 Q206T 0.99 0.91 0.95 1.10 0.8 0.92 206 Q206V 1.01 1.04 1.19 1.11 0.6 1.07 206 Q206W 0.81 0.80 0.69 1.05

0.91 206 Q206Y 1.04 0.96 0.96 1.18 0.9 0.93 207 S207A 0.64 0.84 0.97 0.93

0.95 207 S207C 0.27 0.16

0.49

207 S207D 0.28

207 S207E 0.32

207 S207F 0.29

207 S207G 0.86 0.64 0.62 0.92

0.50 207 S207H

207 S207I

207 S207K 0.37

207 S207L 0.35

207 S207M 0.33 0.21 0.07 0.38

207 S207N

207 S207P 0.44 0.06

207 S207Q 0.19 0.21

207 S207R 0.43

207 S207T 0.65 0.20 0.14 0.42

0.11 207 S207V 0.21 1.19 2.46 0.17

207 S207W 0.25

0.15

207 S207Y 0.25 0.18

0.09

208 T208A 0.89 1.28 1.15 1.12 0.1 1.02 208 T208C 0.82 1.48 1.13 1.24 0.8 1.14 208 T208D 0.27 0.78 0.73 0.35 0.2 0.20 208 T208E 0.25 0.42

208 T208F

208 T208G 0.19

0.2 0.11 208 T208H 0.18

208 T208I

208 T208K 0.24 0.73 0.06

208 T208L 0.87 1.40 1.12 1.14

1.18 208 T208M 0.22 5.66 6.03 1.79 0.4 0.37 208 T208N

208 T208P 0.41 1.68 1.07 1.20

0.69 208 T208Q 0.29 0.15 0.10

208 T208R 0.18

208 T208S 0.81 1.20 1.16 1.01 0.2 1.24 208 T208V 0.62 1.32 1.44 1.20

0.94 208 T208W 0.17

208 T208Y 0.19

0.73

209 L209A 1.06 0.51 0.27 0.77 0.6 0.43 209 L209C 0.82 1.41 1.04 1.05 0.9 1.53 209 L209D

209 L209E 0.98 0.69 0.36 0.76 0.8 0.71 209 L209F 0.72 1.26 1.05 1.15 0.2 2.25 209 L209G 1.00 0.51 0.33 0.60 0.3 0.26 209 L209H 0.64 0.45 0.25 0.62 0.6 0.14 209 L209I

209 L209K 0.88 0.81 0.69 1.05 0.3 1.20 209 L209M 0.71 1.26 1.09 1.16 0.8 1.83 209 L209N

209 L209P 0.22 1.24 0.26

209 L209Q 0.84 0.97 0.44 0.89 0.7 0.99 209 L209R 0.81 0.63 0.31 0.90

0.65 209 L209S 0.99 0.52 0.27 0.63 0.5 0.36 209 L209T 0.81 0.77 0.35 0.82 0.5 0.88 209 L209V 0.83 1.20 1.01 1.00 0.6 0.82 209 L209W 0.78 1.43 0.96 1.11 0.3 1.27 209 L209Y 0.62 0.95 0.64 1.01 0.1 1.47 210 P210A 0.66 1.12 0.81 0.89 0.3 0.93 210 P210C 0.42 1.52 0.90 0.96 0.2 0.75 210 P210D 0.32 1.40 0.78 1.18 0.1 0.26 210 P210E 0.37 1.67 1.08 1.31 0.4 0.69 210 P210F 0.21 10.28 3.47 2.00 0.1 0.11 210 P210G 0.32 1.78 1.00 1.26

0.58 210 P210H

210 P210I 0.46 1.04 0.88 1.19

0.61 210 P210K 0.33 1.08 0.84 1.28

0.60 210 P210L 0.20

15.17 

0.31 210 P210M 0.29 1.15 1.11 1.48

0.43 210 P210N

210 P210Q 0.27 2.95 2.26 2.01

0.84 210 P210R 0.23 3.30 2.81 2.38

0.46 210 P210S 0.58 1.35 1.10 1.15 0.4 1.25 210 P210T 0.55 1.15 1.10 1.34 0.3 1.10 210 P210V 0.49 1.36 1.24 1.13 0.2 0.75 210 P210W 0.18

0.1 0.12 210 P210Y 0.24 0.34 0.17 0.21

211 G211A 0.90 1.54 1.09 1.04 1.0 0.92 211 G211C 1.13 0.68 1.18 0.94 1.1 0.86 211 G211D 0.95 1.52 1.15 0.99 1.4 0.95 211 G211E 0.92 1.31 1.08 1.10 1.3 0.90 211 G211F 0.85 1.21 1.09 1.15 0.6 1.08 211 G211H

211 G211I

211 G211K 0.90 1.05 0.90 0.95 0.4 1.03 211 G211L 0.67 1.22 1.18 1.12 0.7 0.86 211 G211M 0.88 1.22 1.21 0.99 0.9 0.96 211 G211N 0.92 1.29 1.12 1.00 1.0 0.99 211 G211P 0.86 1.32 1.66 1.01 0.6 0.99 211 G211Q 0.77 1.26 1.01 1.18 1.0 1.07 211 G211R 0.76 0.67 0.81 0.96 0.2 0.92 211 G211S 0.95 1.25 1.18 1.01 0.9 1.01 211 G211T 0.78 1.37 1.35 1.15 0.7 1.07 211 G211V 0.76 1.33 1.20 0.92 0.5 0.93 211 G211W 0.80 1.33 1.08 1.18 0.2 1.04 211 G211Y 0.86 1.01 1.27 1.16 0.8 1.04 212 N212A 1.18 0.98 1.29 0.99 0.8 0.67 212 N212C 1.06 1.04 1.20 0.92 0.9 1.13 212 N212D

212 N212E 0.97 1.44 1.12 0.93 1.2 0.75 212 N212F 1.08 0.91 1.01 0.95 0.5 0.75 212 N212G 0.80 1.14 1.32 0.98 0.9 0.92 212 N212H 0.95 1.22 1.11 0.94 0.6 1.21 212 N212I 0.49 0.41 0.41 0.24 0.5 0.20 212 N212K 0.79 0.82 0.75 0.99 0.1 0.85 212 N212L 0.83 0.63 0.69 0.76 0.2 0.75 212 N212M 1.06 1.08 1.04 1.09 0.5 0.87 212 N212P 0.99 0.96 0.85 1.00 0.3 0.78 212 N212Q 0.95 0.97 0.80 0.89 0.9 0.98 212 N212R 0.83 0.74 0.79 1.06 0.2 0.83 212 N212S 1.09 1.12 0.96 1.03 0.8 0.77 212 N212T 0.23 6.10 4.36 2.96 0.6 1.31 212 N212V 0.77 0.97 0.99 1.08 0.6 0.83 212 N212W

212 N212Y 0.93 1.05 0.85 0.96 0.4 0.98 213 K213A 1.05 1.23 1.22 0.95 1.4 0.91 213 K213C 0.96 1.03 1.03 0.86 1.4 0.99 213 K213D 1.01 1.13 1.20 0.89 1.4 0.86 213 K213E 0.96 0.99 1.09 0.89 1.5 0.84 213 K213F 0.92 1.20 1.26 0.98 1.1 0.93 213 K213H 1.01 1.29 1.07 0.97 1.3 1.09 213 K213I 1.02 1.01 1.14 0.94 1.2 0.96 213 K213L 1.03 1.13 1.17 1.03 1.3 1.17 213 K213M 1.06 1.13 1.17 1.04 1.5 1.03 213 K213N 1.02 1.26 1.17 1.00 1.7 0.95 213 K213Q 1.04 1.36 1.01 0.97 1.5 1.04 213 K213R 0.78 1.24 1.15 0.83 1.2 0.98 213 K213S 0.82 1.17 1.07 0.96 1.5 0.85 213 K213T 0.91 1.35 1.21 0.85 1.5 0.94 213 K213V 0.85 1.16 1.16 1.06 1.1 0.99 213 K213W 0.80 1.11 1.10 0.98 0.9 1.13 213 K213Y 0.85 1.15 1.01 0.97 1.3 0.96 214 Y214A 0.17 2.41 1.57 0.71 0.2 0.07 214 Y214C 0.54 0.95 0.82 0.84

0.64 214 Y214D 0.18 3.22 3.18 1.71 0.2 0.12 214 Y214F 0.97 1.15 1.14 0.95

0.87 214 Y214G 0.20 0.38

0.07

214 Y214H 0.36 1.23 1.03 1.28

0.81 214 Y214I 0.86 1.04 1.05 1.01

0.95 214 Y214K 0.15

0.3 0.07 214 Y214L 0.73 1.10 0.92 0.97

0.84 214 Y214M 0.41 0.85 0.74 1.02

0.33 214 Y214N 0.19 1.65 1.59 1.29 0.7 0.18 214 Y214P 0.22 2.06 2.29 1.41

0.72 214 Y214Q 0.36 1.27 0.76 0.95

0.51 214 Y214R 0.18 0.80 0.28 0.12

214 Y214S 0.18 2.22 1.06 1.50 0.2 0.10 214 Y214T 0.50 1.03 0.90 0.98

0.81 214 Y214V 0.65 1.01 0.94 0.97

0.91 214 Y214W 0.69 1.24 1.01 1.15

0.91 215 G215A 0.99 1.16 0.99 0.98 0.6 0.58 215 G215C 1.00 1.03 1.06 0.82 0.8 0.70 215 G215D 0.89 1.33 1.10 1.06 1.0 0.70 215 G215E 1.04 1.22 1.16 0.84 1.0 0.75 215 G215F

215 G215H 0.64 1.16 0.76 1.05 0.1 0.72 215 G215I 0.56 1.23 0.85 1.09

0.64 215 G215K 0.95 0.95 0.77 0.95

0.62 215 G215L 0.26 0.07

0.12

215 G215M 0.72 1.23 1.00 0.82 0.1 0.59 215 G215N 0.70 1.11 1.07 0.97

0.63 215 G215P 0.34

215 G215Q 0.80 1.37 0.96 0.97 0.1 0.67 215 G215R 0.74 0.76 0.74 0.83

0.66 215 G215S 0.84 1.12 0.94 0.93 0.1 0.72 215 G215T 0.61 1.07 0.96 1.07

0.83 215 G215V 0.36 1.52 0.90 1.15 0.1 0.51 215 G215W 0.48 1.00 0.88 0.91 0.1 0.71 215 G215Y 0.49 1.04 0.77 1.05

0.64 216 A216C 0.97 1.21 1.11 0.92 1.2 0.89 216 A216D 0.76 1.22 1.28 1.19 1.2 0.95 216 A216E 1.20 1.36 0.92 1.03 1.4 0.75 216 A216F 1.22 1.20 1.21 0.87 1.2 0.91 216 A216G 1.00 0.99 0.78 0.88 0.8 0.90 216 A216H 1.03 0.86 1.01 0.93 0.9 0.79 216 A216I 1.17 0.92 0.94 1.01 1.0 0.81 216 A216K 0.94 0.78 0.98 0.87 1.0 0.55 216 A216L 0.96 0.90 0.78 0.83 0.9 1.05 216 A216M 0.82 0.85 1.07 0.90 1.1 0.82 216 A216N 1.03 0.97 1.11 1.07 1.1 0.72 216 A216P 0.90 1.09 0.94 1.11 1.2 1.00 216 A216Q 1.03 0.96 1.14 1.09 0.9 0.94 216 A216R 1.12 0.54 0.62 0.92 0.1 0.90 216 A216S 0.73 1.00 1.09 1.22 0.9 1.03 216 A216T

216 A216V 0.92 1.13 0.93 0.94 0.9 1.15 216 A216W 0.96 0.55 0.86 0.77 0.9 0.73 216 A216Y 0.81 0.76 0.90 0.96 1.1 0.88 217 Y217A 0.38 0.16 0.08 0.14

217 Y217C 1.03 0.98 0.86 0.95 1.6 1.34 217 Y217D 1.01 1.13 1.07 1.21 1.1 0.34 217 Y217E 1.00 1.40 0.99 1.18 1.3 0.54 217 Y217F 1.04 0.99 1.03 0.97 1.0 1.35 217 Y217G 0.85 0.81 0.72 0.95 1.0 0.97 217 Y217H 0.96 0.97 0.90 1.15 1.1 0.76 217 Y217I 0.84 1.16 1.24 1.14 0.7 1.53 217 Y217K 1.02 0.80 0.58 0.97 1.0 1.06 217 Y217L 0.98 1.34 0.97 1.07 1.4 3.46 217 Y217M 0.93 1.31 1.22 1.07 1.5 1.80 217 Y217N 0.78 0.94 0.65 0.91 1.0 1.21 217 Y217P 0.28 0.54 0.18 0.57 0.1 0.18 217 Y217Q 0.92 1.19 1.29 1.11 1.2 1.05 217 Y217R 1.00 0.80 0.54 1.01 0.9 0.87 217 Y217S 0.83 1.11 0.95 1.01 1.0 1.63 217 Y217T 0.80 1.03 0.63 1.10 0.8 1.15 217 Y217V 0.75 1.10 0.98 1.22 0.7 1.03 217 Y217W 0.80 0.76 0.68 0.79 1.0 0.71 218 N218A 0.99 0.94 0.92 0.97 0.7 1.13 218 N218C 1.05 1.06 0.86 0.83 1.1 0.76 218 N218D

218 N218E 0.90 1.03 1.09 0.85 1.1 0.59 218 N218F 0.77 0.62 0.55 0.78 0.2 0.97 218 N218G 0.88 1.06 1.07 1.01 0.5 1.23 218 N218H 0.94 1.02 0.93 0.91 0.9 0.61 218 N218I 0.52 0.45 0.43 0.57 0.1 0.36 218 N218K 0.76 0.55 0.59 0.93

1.14 218 N218L 0.46 0.66 0.69 0.64

0.62 218 N218M 0.76 0.95 0.74 0.75 0.4 0.94 218 N218P 0.29 1.56 0.82 1.19 0.2 0.60 218 N218Q

218 N218R 0.65 0.54 0.45 0.69

1.16 218 N218S 1.00 1.00 0.99 1.07 1.2 1.07 218 N218T 0.93 0.62 0.73 0.73 0.9 0.58 218 N218V 0.48 0.51 0.64 0.50 0.2 0.77 218 N218W 0.70 0.65 0.59 0.65 0.3 0.68 218 N218Y 0.70 0.62 0.75 0.70 0.2 1.08 219 G219A 0.82 0.14

0.08 0.3 0.19 219 G219C 0.53 0.83 0.71 0.65 1.0 0.60 219 G219D 0.46

0.4 0.23 219 G219E 0.33 0.09

3.4 0.40 219 G219F 0.35

0.07

0.1 0.48 219 G219H 0.46

0.07

0.7 0.08 219 G219I 0.24 0.10 0.31

0.4 0.12 219 G219K 0.27 0.27

0.08

0.41 219 G219L 0.54 0.68 0.70 0.70 0.2 0.89 219 G219M 0.32 0.21

0.06 0.7 0.44 219 G219N

219 G219P 0.22 0.20

1.0 0.65 219 G219Q 0.31 0.35

1.3 0.42 219 G219R 0.26 0.30 0.08

0.7 0.43 219 G219S 1.04

0.9 0.19 219 G219T 0.22 0.28 0.34 0.08 0.8 0.58 219 G219V 0.25 0.22

0.5 0.57 219 G219W 0.27 0.15

0.6 0.55 219 G219Y 0.32 0.18

0.5 0.45 220 T220A 0.58 0.71 0.89 1.12

220 T220C 0.63 0.69 0.53 0.71

220 T220D 0.86 0.27 0.32 0.30

220 T220E 0.59

0.18

220 T220F 0.28 0.08 0.15 0.06

220 T220G 0.53 0.19 0.06 0.40

220 T220H

220 T220I 0.28

220 T220K 0.26

220 T220L 0.26

0.29 0.14

220 T220M 0.42

220 T220N 0.36 0.07

0.13

220 T220P 0.26 0.10 0.26

220 T220Q 0.33 0.07

220 T220R 0.28 0.14

0.07

220 T220S 0.68 1.16 1.13 0.97 0.6 0.49 220 T220V 0.38 0.39 0.41 0.76

220 T220W 0.31 0.06 0.07

220 T220Y 0.29

0.06

221 S221A 1.12

221 S221C 1.84

221 S221D 2.07

221 S221E 1.82

221 S221G 1.34

221 S221H 1.05

221 S221K 0.43

221 S221L 0.39

221 S221M 0.41

221 S221N 1.64

221 S221P 0.40

221 S221Q 0.85

221 S221R 0.36 0.08

221 S221T 1.09

221 S221V 0.34

221 S221W 0.37

222 M222A 1.49 0.94 0.68 0.92 1.0 0.48 222 M222C 1.15 0.66 0.55 0.80 1.6 1.32 222 M222D 0.65 0.56 0.48 0.80

222 M222E 0.95 0.90 0.46 1.03

222 M222F 0.86 0.62 0.73 1.00 1.4 0.06 222 M222H 1.07 0.52 0.56 0.78 2.0 0.06 222 M222I 1.19 0.68 0.66 1.02

222 M222K 1.59 0.25 0.20 0.50

222 M222L 0.98 0.48 0.60 0.76 0.6 0.13 222 M222N 1.14 0.76 0.74 0.93 0.9 0.27 222 M222P 1.22 0.47 0.24 0.54 0.3 0.14 222 M222Q 0.78 0.97 0.87 1.19 1.4 0.12 222 M222R

222 M222S 1.15 0.77 0.62 0.87 1.0 0.95 222 M222T 1.12 0.64 0.46 0.72 1.0 0.34 222 M222V 1.20 0.69 0.50 0.80 0.9 0.12 222 M222W 1.89 0.36 0.21 0.74 0.7 0.09 222 M222Y 1.46 0.55 0.34 0.88

223 A223C 0.36 0.60 0.54 0.50

0.14 223 A223D

223 A223E 0.24 0.20

0.10

223 A223F 0.23 0.42

0.07

223 A223G 0.62 1.00 0.60 0.86 0.2 0.66 223 A223H 0.25 0.20

0.09

223 A223I

223 A223K 0.24 0.28

0.16

223 A223L 0.26 0.35 0.07

223 A223M 0.27 0.26

223 A223N

223 A223P 0.26 0.61 0.31 0.11

223 A223Q 0.43

223 A223R 0.24 0.30

0.08

223 A223S 1.05 0.95 1.00 0.91 0.9 0.72 223 A223T 0.23 1.22 0.73 0.91 0.2 0.17 223 A223V 0.17

0.07

223 A223W 0.22 1.54 0.83 0.23

223 A223Y 0.20

0.45 0.73

224 S224A 1.14 1.24 1.14 1.15 0.9 1.16 224 S224C 1.34 1.23 1.23 1.22 1.1 0.65 224 S224D 0.22 1.59 0.58 0.29

224 S224E 0.30 0.30

0.14

224 S224F 0.23 0.62

0.13

224 S224G 0.90 1.23 1.15 1.13 0.3 0.63 224 S224H 0.27 0.19

224 S224I 0.19

80.86 

224 S224K

224 S224L 0.20

4.61

224 S224M 0.26 0.30

0.10

224 S224N 0.35 1.77 1.55 1.26 0.6 0.24 224 S224P 0.38 0.36 0.24 0.42

224 S224Q 0.25 2.04 0.13 0.17

224 S224R 0.24 0.62

224 S224T 0.66 1.16 1.22 1.07 0.9 0.37 224 S224V 0.97 0.89 0.90 1.05 0.9 0.06 224 S224W 0.25 0.32 0.19 0.06

224 S224Y 0.24 0.20

0.13

225 P225A 1.38 0.24 0.34 0.55

225 P225C 0.88 0.21 0.30 0.46

225 P225D

225 P225E 0.22

0.10

225 P225F 0.24 0.35

0.12

225 P225G 1.06 0.42 0.38 0.49

225 P225H 0.28

225 P225I 0.61 0.19 0.23 0.34

225 P225K 0.24 0.08

0.06

225 P225L 0.24

0.07

225 P225M 0.30 0.26 0.34 0.26

225 P225N

225 P225Q 0.29 0.16 0.40 0.16

225 P225R 0.23 0.16

0.14

225 P225S 1.13 0.37 0.40 0.55 0.9 0.07 225 P225T 0.79 0.25 0.29 0.47

225 P225V 0.77 0.43 0.37 0.50

225 P225W 0.22 0.27

0.17

225 P225Y 0.32

0.07

226 H226A

226 H226C 0.75 1.15 1.26 0.89

1.25 226 H226D 0.31

226 H226E 0.22 1.54 1.86 1.16

0.53 226 H226F 0.81 1.08 1.25 1.11

0.70 226 H226G 0.60 1.07 0.91 1.13

0.88 226 H226I 0.42 1.07 1.39 1.04

0.84 226 H226K 0.16

3.21 0.1 0.15 226 H226L 0.55 0.99 1.00 1.07

0.94 226 H226M 0.76 1.19 1.16 0.96

0.97 226 H226N 0.51 1.19 1.11 1.21

0.84 226 H226P 0.27

226 H226Q

226 H226R 0.30

0.09

226 H226S 0.77 1.26 1.20 1.08

1.06 226 H226T 0.37 1.35 1.44 1.16

0.90 226 H226V 0.34 1.06 1.36 1.01

1.20 226 H226W 0.16

3.77

0.19 226 H226Y 0.73 1.22 0.97 1.06

0.66 227 V227A 1.03 0.99 1.26 0.83 1.0 0.81 227 V227C 0.95 1.01 1.29 1.01 0.9 0.81 227 V227D 0.40

0.06

227 V227E 0.31

227 V227F 0.30 0.87 1.35 1.00 0.5 0.74 227 V227G 0.32 1.55 1.43 1.06 0.9 0.69 227 V227H 0.34

227 V227I 0.97 1.12 1.06 0.82 0.7 0.95 227 V227K 0.34

227 V227L 0.50 1.36 1.30 1.04 0.4 0.92 227 V227M 0.36 0.76 1.18 0.87 0.7 0.75 227 V227N 0.30

227 V227P 0.27

0.06

227 V227Q 0.27

0.07

227 V227R 0.29

0.08

227 V227S 0.16 14.70  19.48  4.22 0.5 0.53 227 V227T 0.63 1.04 1.44 1.01 0.7 0.87 227 V227W 0.25

0.14

1.5 0.06 227 V227Y

228 A228E 0.48

228 A228F 0.46

228 A228G 0.38 1.14 1.11 1.31 1.0 0.66 228 A228H 0.51

228 A228I 0.23 1.27 0.90 1.50 0.2 0.23 228 A228K 0.45

228 A228L 0.31 0.14

0.09

228 A228M 0.22 0.86 0.93 1.15 0.4 0.20 228 A228N 0.49

228 A228P 0.58

228 A228R 0.48

228 A228S 0.88 0.86 1.10 1.17 1.1 0.80 228 A228T 0.78 1.04 1.04 1.07 1.0 0.68 228 A228V 0.37 1.18 1.37 1.39 0.9 0.51 228 A228W 0.46 0.06

228 A228Y 0.39

229 G229A 1.20 0.82 1.12 0.99 0.8 0.99 229 G229C 0.23

0.12

229 G229D 0.14

0.6 0.11 229 G229E 0.29

229 G229F 0.35

229 G229H 0.28

229 G229I 0.27

229 G229K 0.30

0.07

229 G229L 0.19

0.49 0.12

229 G229M 0.21

0.13

229 G229N 0.25

229 G229P 0.28

229 G229Q 0.31

229 G229R 0.29

0.13

229 G229S 0.76 0.75 0.96 1.03 0.6 1.03 229 G229T 0.12

0.6 0.15 229 G229V 0.20

0.19 0.07

229 G229W 0.25

229 G229Y 0.24

230 A230C 1.06 0.88 1.21 1.12 0.8 1.06 230 A230D

230 A230E 0.77 0.74 1.09 1.06 0.6 0.75 230 A230F 0.50 0.52 1.30 1.06 1.1 0.94 230 A230G 0.99 0.86 1.16 0.95 1.0 0.98 230 A230H 0.16 10.35  16.17  3.82 0.1 0.38 230 A230I 0.24 1.02 1.83 1.31

0.83 230 A230K 0.26

230 A230L 0.27

0.12

230 A230M 0.24 1.19 1.78 1.27

0.66 230 A230N 0.19 1.80 2.19 1.72 0.6 0.58 230 A230P 0.24

0.10

230 A230Q 0.39 0.81 1.14 1.03 0.3 0.86 230 A230R 0.31

0.06

230 A230S 1.00 0.86 1.00 1.00 0.9 1.04 230 A230T 0.89 0.94 0.94 1.01 0.7 1.14 230 A230V 0.56 0.85 0.95 1.08 0.2 1.17 230 A230W 0.15 0.58

230 A230Y 0.11 0.06

231 A231C 0.84 0.99 1.15 1.09 0.8 0.79 231 A231D 0.21

0.07

231 A231E 0.31

231 A231F 0.33 1.16 1.34 1.33 0.5 0.57 231 A231G 0.42 1.10 1.04 1.35 1.1 0.86 231 A231H 0.32

0.07

231 A231I 0.86 1.08 1.16 1.12 0.8 0.71 231 A231K 0.49

231 A231L 0.45 1.07 1.27 1.32 0.7 0.83 231 A231M 0.41 1.15 1.26 1.30 0.7 0.73 231 A231N 0.31 0.09

231 A231P 0.53

231 A231Q 0.31

231 A231R 0.48

231 A231S 0.55 0.96 1.28 1.14 1.0 1.03 231 A231T 0.57 1.22 1.31 1.09 0.8 0.98 231 A231V 0.71 1.07 1.04 1.12 0.8 0.99 231 A231W 0.18 4.36 5.85 4.42 0.3 0.16 231 A231Y 0.25 1.52 2.14 1.63 0.2 0.44 232 A232C 0.92 1.09 1.13 1.00 0.9 0.99 232 A232E 0.28 0.25 0.21 0.37 1.0 0.14 232 A232H 0.22

0.13

232 A232K 0.37

232 A232L 0.37 1.15 1.29 1.42 1.1 0.87 232 A232M 0.66 1.02 1.04 0.98 1.0 0.91 232 A232N 0.20 1.64 2.16 1.52 1.1 0.44 232 A232P 0.30

232 A232Q 0.54

232 A232S 0.81 0.96 1.27 0.93 0.9 0.94 232 A232T 0.73 0.97 1.02 1.03 1.0 1.04 232 A232V 0.77 1.00 1.35 0.99 1.0 1.09 232 A232Y 0.43

233 L233D 0.71 0.89 0.91 0.92 1.1 0.71 233 L233F 0.38

233 L233H 0.24

233 L233I 0.85 0.89 1.11 1.03 1.0 0.90 233 L233M 0.67 0.92 0.99 1.01 0.9 0.94 233 L233P 0.40

233 L233R 0.49 0.07

233 L233S 0.61 1.05 1.16 0.96 0.9 0.78 233 L233T 0.78 0.95 1.25 0.90 1.0 0.89 233 L233V 0.94 1.15 1.09 0.89 1.1 0.91 233 L233Y 0.38

234 I234A 1.16 0.86 0.96 0.88 0.8 1.12 234 I234C 1.21 1.02 0.92 0.96 1.1 0.88 234 I234D 0.21 0.70 1.52 0.91 0.6 0.44 234 I234E 0.88 1.05 1.01 0.86 0.8 1.01 234 I234F 0.72 1.03 1.02 0.72 0.1 1.02 234 I234G 0.33 0.93 0.96 1.15 0.7 0.86 234 I234H 0.37 0.98 0.98 0.97 0.3 0.94 234 I234K 0.30 0.89 0.92 1.00 0.1 0.84 234 I234L 1.22 0.82 0.84 1.08 1.1 1.07 234 I234M 1.27 1.02 0.91 0.98 1.0 1.18 234 I234N 0.42 1.08 0.98 1.03 0.9 0.91 234 I234P 0.29

234 I234Q 0.87 0.72 0.94 0.93 0.9 0.96 234 I234R 0.14

0.2 0.34 234 I234S 0.81 0.92 0.93 0.93 0.9 0.98 234 I234T 1.14 0.87 0.92 1.02 1.1 0.99 234 I234V 1.20 1.02 1.19 0.93 1.1 1.14 234 I234W 0.17 4.77 6.83 2.41 0.1 0.19 234 I234Y 0.39 0.88 1.06 0.82

0.95 235 L235A 0.67 1.05 0.95 1.05 1.0 1.15 235 L235C 1.08 0.96 1.24 1.03 0.9 1.07 235 L235D 0.20 0.19 1.17 0.45 1.1 0.14 235 L235E 0.42 0.81 1.03 0.94 1.1 0.25 235 L235F 1.25 1.08 1.01 0.94 1.0 0.80 235 L235G 0.27 1.09 0.76 1.11 1.1 0.62 235 L235H

235 L235I 1.31 0.92 0.83 1.10 1.1 0.94 235 L235K 1.32 0.86 1.21 0.96 1.1 0.85 235 L235M 1.34 0.99 0.99 1.03 1.1 0.89 235 L235N 0.25 1.32 1.54 1.19 1.2 0.69 235 L235P 0.31

235 L235Q 1.01 0.92 0.84 1.03 1.1 1.24 235 L235R 1.29 0.79 0.86 0.95 1.0 0.90 235 L235S 0.69 1.05 0.86 0.76 1.0 1.00 235 L235T 0.65 1.10 0.80 0.86 1.1 1.07 235 L235V 1.17 0.92 1.07 0.83 1.1 1.24 235 L235W 1.09 0.98 0.63 1.13 1.1 0.94 235 L235Y 0.99 0.99 0.98 1.04 1.1 1.02 236 S236A 1.21 1.02 1.06 0.94 0.9 1.03 236 S236C 1.28 0.89 0.95 0.96 1.0 0.90 236 S236D 1.22 1.02 0.95 0.98 1.2 1.07 236 S236E 1.26 0.90 0.88 1.09 1.2 1.55 236 S236F

236 S236G 1.20 1.06 1.09 0.97 0.9 0.99 236 S236H 1.12 0.84 0.87 0.92 1.2 1.07 236 S236I

236 S236K 0.31 0.96 0.80 1.18 0.7 0.55 236 S236L 0.19 0.42 0.92 0.66 0.8 0.13 236 S236M

236 S236N 1.24 1.03 1.18 0.86 0.6 1.13 236 S236P 0.34

0.09

236 S236Q 1.18 0.85 0.69 0.95 1.1 1.00 236 S236R 0.34 0.96 0.72 1.13 0.7 0.60 236 S236T 0.59 0.99 0.97 1.04 0.8 1.16 236 S236V 0.91 0.97 0.86 1.06 0.9 1.21 236 S236W 0.18 2.11 3.43 2.28 0.8 0.50 236 S236Y 0.48 1.10 0.66 0.91 0.8 1.09 237 K237A 1.13 1.11 1.31 0.81 1.0 1.03 237 K237C 0.19 1.21 1.50 0.91 1.1 0.33 237 K237D

237 K237E 1.03 0.86 0.84 0.85 1.0 1.22 237 K237F 1.05 0.80 0.99 0.92 1.0 1.21 237 K237G 1.05 0.90 1.08 1.06 1.0 0.94 237 K237H 1.05 0.91 0.97 0.93 1.1 0.88 237 K237I 1.02 1.03 0.69 0.70 1.0 1.05 237 K237L 1.04 0.96 0.89 1.10 1.0 1.12 237 K237M 1.17 0.89 1.09 0.86 0.9 1.20 237 K237N 1.09 1.00 0.99 0.94 1.1 0.93 237 K237P 0.19 0.50 0.92 0.59 1.1 0.15 237 K237Q 1.12 0.74 0.87 0.84 1.1 1.01 237 K237R 1.13 0.82 0.95 1.02 1.0 1.08 237 K237S 1.17 0.97 1.07 0.86 1.0 1.24 237 K237T 1.07 0.81 0.75 0.82 1.0 0.94 237 K237V 1.08 0.85 1.09 1.10 0.9 1.09 237 K237W 0.81 0.96 1.08 0.95 0.9 0.87 237 K237Y 1.00 1.10 0.98 1.08 0.9 1.10 238 H238A 0.28 1.34 1.44 1.12 1.1 0.46 238 H238C 0.62 1.07 1.09 0.99 1.1 0.97 238 H238D 0.35 0.93 1.18 1.19 1.1 0.78 238 H238E 0.61 0.91 1.00 1.00 1.1 1.08 238 H238F 0.74 0.69 1.05 0.95 1.1 1.09 238 H238G 0.22 5.21 5.98 2.44 1.0 0.44 238 H238I 0.22 7.74 7.02 3.64 1.1 0.52 238 H238K 0.87 0.82 1.07 0.89 1.0 1.24 238 H238L 0.20

4.71 1.2 0.36 238 H238M 0.58 1.00 1.15 0.89 1.0 0.93 238 H238N

238 H238P 0.17

238 H238Q

238 H238R 0.79 0.96 0.76 1.04 0.9 1.17 238 H238S 0.55 1.29 1.03 0.82 1.0 0.99 238 H238T 0.16

238 H238V 0.20

12.14  0.9 0.26 238 H238W 0.41 1.14 0.92 1.16 1.1 1.10 238 H238Y

239 P239A 0.57 0.98 0.94 0.88 1.0 0.86 239 P239C 0.78 0.96 0.85 0.83 1.0 1.03 239 P239D 0.89 1.00 0.81 0.98 1.1 0.87 239 P239E 0.80 1.16 0.81 0.97 1.1 0.96 239 P239F 0.66 1.15 0.67 1.03 1.0 1.02 239 P239G 0.76 0.71 0.48 0.95 0.2 0.79 239 P239H 0.89 1.41 1.02 1.12 1.1 1.09 239 P239I

239 P239K 0.23 0.15

0.10

239 P239L 0.65 1.04 0.90 0.95 1.1 1.09 239 P239M 0.79 1.12 0.70 0.98 1.1 0.89 239 P239N 0.82 1.08 0.83 1.01 1.2 0.94 239 P239Q 0.91 1.14 0.80 1.10 1.2 0.97 239 P239R 0.92 1.21 0.67 1.27 1.0 1.04 239 P239S 0.87 1.31 0.96 0.99 1.1 1.33 239 P239T 0.80 0.97 1.07 1.11 1.2 1.03 239 P239V 0.71 1.10 1.22 1.06 1.2 1.32 239 P239W 0.65 1.06 0.75 1.11 1.0 1.28 239 P239Y 0.76 0.90 0.94 1.20 1.2 1.22 240 N240A 0.80 0.96 0.99 0.96 1.0 0.91 240 N240C 1.06 1.04 0.83 0.89 1.1 0.95 240 N240D 1.05 1.07 0.88 1.03 1.2 0.93 240 N240E 1.03 1.27 0.83 1.00 1.2 1.05 240 N240F 1.02 0.94 0.84 0.93 1.1 0.92 240 N240G 1.03 1.21 0.87 0.90 1.0 1.01 240 N240H

240 N240I

240 N240K 1.09 1.04 1.04 0.99 1.1 1.02 240 N240L 0.78 1.27 0.86 1.08 1.0 1.05 240 N240M 0.94 1.03 0.76 0.92 1.0 0.94 240 N240P 0.39 0.75 0.72 0.89 0.9 0.54 240 N240Q 0.91 1.09 0.88 1.11 1.1 1.04 240 N240R 0.75 0.85 0.59 1.14 1.0 0.97 240 N240S 1.00 1.19 1.04 1.11 1.1 0.95 240 N240T 0.90 1.02 0.77 1.14 1.1 1.02 240 N240V 0.90 1.06 0.92 1.06 1.0 1.10 240 N240W 1.05 1.05 0.66 1.01 1.0 1.00 240 N240Y 0.92 1.01 0.80 1.22 1.0 1.43 241 W241A 0.84 0.94 0.65 1.02 1.1 0.86 241 W241C 0.63 0.96 0.72 0.98 1.1 1.09 241 W241D 0.44 1.06 1.03 1.05 1.2 0.89 241 W241E 0.34 1.05 0.81 1.06 1.1 0.63 241 W241F 0.81 0.94 0.86 0.75 1.0 0.87 241 W241G 0.31 1.35 1.05 0.92 1.0 0.64 241 W241H 0.65 1.08 0.99 1.12 1.1 1.05 241 W241I 0.75 1.11 0.99 1.13 1.0 1.15 241 W241K 0.83 1.00 0.88 1.22 1.0 1.11 241 W241L 0.85 0.78 1.00 1.03 1.0 0.99 241 W241M 0.91 1.01 0.82 1.04 1.1 1.07 241 W241N 0.35 1.14 0.92 1.07 1.2 0.64 241 W241P 0.18

0.9 0.30 241 W241Q 0.65 1.40 1.00 1.14 1.1 1.14 241 W241R 0.59 0.93 0.88 1.12 0.9 1.37 241 W241S 0.66 1.14 0.68 1.04 0.9 1.06 241 W241T 0.61 1.06 0.86 1.16 1.0 1.11 241 W241V 0.61 1.20 1.01 1.09 1.0 1.35 241 W241Y 0.81 1.17 0.84 1.08 1.0 1.38 242 T242A 1.24 0.92 1.10 0.95 1.1 0.75 242 T242C 1.10 0.89 1.21 0.84 1.1 0.86 242 T242D

242 T242E 1.03 1.08 1.32 0.87 1.0 0.90 242 T242F 0.71 0.86 0.97 0.81 0.9 0.99 242 T242G 0.88 0.74 1.02 1.03 1.0 0.95 242 T242H 0.95 1.14 0.98 0.90 1.1 0.92 242 T242I 0.84 0.82 1.26 1.11 1.1 0.93 242 T242K 0.99 0.77 1.07 0.93 1.1 0.94 242 T242L 0.97 0.99 1.12 1.01 1.1 0.89 242 T242M 1.00 0.83 1.03 0.97 1.0 0.87 242 T242N 1.02 0.65 1.14 0.96 1.1 0.92 242 T242P 0.93 0.83 1.22 1.06 1.1 0.97 242 T242Q 0.91 0.87 1.34 0.95 1.1 1.23 242 T242R 0.91 1.04 1.18 0.91 1.1 1.05 242 T242S 1.05 1.00 1.16 1.18 1.1 0.95 242 T242V 0.80 0.89 1.20 0.99 1.0 1.05 242 T242W 0.62 0.72 0.97 0.91 1.1 0.96 242 T242Y 0.69 0.94 0.97 1.01 1.1 1.02 243 N243A

243 N243C 1.05 0.88 1.22 0.98 1.0 0.93 243 N243D

243 N243E 1.14 0.94 1.22 0.98 1.1 0.79 243 N243F 0.69 0.75 1.03 1.01 0.6 0.79 243 N243G 0.97 1.16 0.94 1.00 1.2 0.72 243 N243H 0.26

243 N243I 0.94 0.79 1.61 0.79 0.8 0.91 243 N243K 0.78 0.97 1.05 1.11 0.9 0.85 243 N243L 0.83 0.92 1.24 1.03 0.8 0.74 243 N243M

243 N243P 0.26

0.19

243 N243Q 0.93 0.74 1.28 1.03 1.0 0.94 243 N243R 0.73 0.79 0.92 0.90 0.8 1.09 243 N243S 0.97 1.05 1.13 0.86 1.0 0.93 243 N243T 0.92 0.97 1.01 0.92 1.0 0.98 243 N243V 0.89 0.87 1.13 1.13 1.0 1.29 243 N243W 0.59 0.90 1.02 1.01 0.6 1.05 243 N243Y 0.81 0.82 1.20 0.82 0.9 0.92 244 T244A 1.53 0.66 0.97 1.07 1.0 0.84 244 T244C

244 T244D 1.13 0.97 1.23 1.13 1.0 1.11 244 T244E 0.69 0.89 1.12 0.90 1.0 0.92 244 T244F 0.83 0.97 0.97 1.01 1.0 0.96 244 T244G 1.05 0.83 1.06 1.01 1.0 0.96 244 T244H 1.06 0.90 1.29 1.01 1.1 0.94 244 T244I

244 T244K 1.09 0.76 0.95 1.00 1.0 0.97 244 T244L 0.99 1.07 1.13 0.92 1.1 1.00 244 T244M 1.15 0.94 1.05 1.07 1.0 0.96 244 T244N 1.03 1.20 1.10 1.03 1.1 0.95 244 T244P 0.74 0.89 1.25 1.00 1.0 1.00 244 T244Q 1.04 0.87 1.23 0.94 1.0 1.08 244 T244R 0.96 0.54 1.04 0.91 0.9 1.10 244 T244S 1.04 1.02 1.23 1.07 1.0 0.99 244 T244V 0.90 0.69 1.07 1.04 1.0 1.06 244 T244W 0.88 0.70 1.29 0.94 1.0 1.13 244 T244Y 0.87 0.38 1.03 1.01 1.0 1.10 245 Q245A 1.00 0.92 1.10 0.93 1.1 0.92 245 Q245C 0.80 0.79 1.15 0.93 1.1 0.89 245 Q245D 1.00 0.73 1.19 0.88 1.1 0.90 245 Q245E 1.03 1.00 1.15 0.79 1.2 0.89 245 Q245F 0.80 0.89 1.21 1.00 1.0 0.98 245 Q245G 0.76 1.12 1.17 0.99 1.1 0.99 245 Q245H 0.93 1.01 1.04 0.97 1.1 0.94 245 Q245I 0.83 0.97 1.12 1.01 1.1 0.99 245 Q245K 0.99 0.83 0.82 0.88 1.1 0.96 245 Q245L 0.88 0.77 1.18 0.85 1.1 0.97 245 Q245M 1.06 0.81 1.19 1.10 1.1 0.92 245 Q245N 0.63 0.91 0.96 0.79 1.0 0.82 245 Q245P 0.27 0.47 0.63 0.50 1.0 0.25 245 Q245R 0.76 0.57 0.89 0.97 1.0 1.07 245 Q245S 0.81 0.93 1.19 0.97 0.9 1.14 245 Q245T 0.82 0.90 1.18 1.03 1.0 1.37 245 Q245V 0.72 0.96 1.19 1.06 1.0 1.09 245 Q245W 0.50 0.94 1.00 0.90 0.9 1.08 245 Q245Y 1.06 0.66 1.08 0.99 1.0 1.06 246 V246A 0.53 1.06 1.22 1.01 0.9 0.92 246 V246C 0.64 0.95 1.05 0.92 1.1 1.02 246 V246D 0.44

246 V246E 0.61

246 V246F 0.31 1.18 1.59 1.59 0.8 0.81 246 V246G 0.18 0.46 0.18 0.47 0.5 0.06 246 V246H 0.30

0.07

246 V246I 1.00 1.00 1.11 0.81 1.1 0.95 246 V246K 0.38

246 V246L 0.67 1.05 1.10 0.88 1.0 0.94 246 V246N 0.20 0.32 0.16 0.32 1.2 0.08 246 V246P 0.43

246 V246Q 0.36 0.07 0.11 0.11

246 V246R 0.23 0.08 0.17 0.19

246 V246S 0.23 0.60 0.54 0.81 0.7 0.33 246 V246T 0.74 0.95 1.23 1.04 1.0 1.10 246 V246Y 0.25 0.23 0.41 0.43 0.2 0.15 247 R247A 0.55 0.86 1.05 0.74 0.2 0.70 247 R247C 0.36 1.07 1.40 1.04 0.4 0.64 247 R247D 0.23 0.43 0.88 0.46 0.2 0.15 247 R247E 0.38 0.77 1.02 0.88 0.3 0.59 247 R247F 0.32 0.96 1.09 0.86 0.3 0.65 247 R247G 0.24

247 R247H 0.31 1.31 1.51 1.28 0.3 0.68 247 R247I 0.37 1.16 1.37 1.11 0.2 0.88 247 R247K 0.50 1.01 1.17 1.02 0.5 0.75 247 R247L 0.30 1.65 1.54 1.25 0.1 0.55 247 R247M 0.42 1.07 1.22 0.83 0.2 0.63 247 R247N

247 R247P

247 R247Q

247 R247S 0.37 1.06 1.56 0.93 0.4 0.74 247 R247T 0.44 1.18 1.33 1.11 0.5 0.97 247 R247V 0.40 0.84 1.31 1.01 0.4 0.76 247 R247W 0.32 1.35 1.39 0.95 0.3 0.68 247 R247Y 0.27 1.53 2.24 1.48 0.2 0.90 248 S248A 1.06 1.03 1.21 1.00 1.0 1.25 248 S248C 1.02 0.82 1.09 0.96 1.0 0.91 248 S248D

248 S248E 1.21 0.61 1.11 0.86 1.0 1.02 248 S248F 0.98 0.97 1.11 0.96 0.9 1.52 248 S248G 0.93 1.11 0.97 0.96 0.9 1.10 248 S248H 0.78 1.16 1.10 0.98 1.0 0.99 248 S248I 1.00 1.01 1.23 1.13 0.9 1.20 248 S248K 1.07 0.54 0.99 1.02 0.9 0.98 248 S248L 1.00 0.82 1.08 1.01 0.9 1.18 248 S248M 1.00 0.75 1.31 0.96 1.0 1.05 248 S248N 1.08 0.96 1.19 1.05 1.0 1.01 248 S248P 0.57 1.06 1.39 1.07 0.9 1.00 248 S248Q 1.10 1.01 1.14 0.84 1.0 0.93 248 S248R 1.10 0.47 0.80 0.87 0.9 0.87 248 S248T 0.95 0.93 1.19 0.96 1.0 1.07 248 S248V 0.80 1.16 1.13 1.01 0.8 1.31 248 S248W 0.85 0.87 1.24 1.02 1.1 0.99 248 S248Y 1.31 0.89 1.17 0.94 1.0 0.98 249 S249A 1.07 0.92 1.25 1.02 1.0 0.95 249 S249C 1.14 0.97 1.21 0.92 1.0 0.86 249 S249D 0.97 0.84 1.17 0.90 0.9 1.27 249 S249E

249 S249F 1.14 0.75 0.97 0.95 0.8 0.89 249 S249G 0.72 0.83 1.17 0.98 0.9 1.04 249 S249H 1.10 0.95 0.87 1.12 0.9 0.87 249 S249I 0.92 0.76 1.30 0.99 0.9 0.93 249 S249K 1.08 0.91 0.83 0.87 0.8 0.93 249 S249L 0.99 0.89 1.19 0.91 0.8 1.21 249 S249M 1.07 0.99 1.24 1.11 1.0 1.00 249 S249N 1.00 1.08 1.35 1.06 1.0 0.92 249 S249P

249 S249Q 1.00 0.73 1.06 1.17 0.8 1.12 249 S249R 1.03 0.78 0.87 0.95 0.9 1.00 249 S249T 1.08 0.78 1.17 0.95 0.9 1.13 249 S249V 0.97 0.82 1.18 1.05 0.9 0.99 249 S249W 0.95 0.92 1.09 1.17 0.8 1.06 249 S249Y 0.94 0.80 1.07 0.91 0.9 1.01 250 L250A

250 L250C 0.37 1.06 1.50 1.21 0.9 1.21 250 L250D 0.24

0.13

250 L250E 0.20 2.64

0.06

250 L250F 0.61 1.05 1.44 0.90 0.7 0.96 250 L250G 0.22 0.11

250 L250H 0.22

250 L250I 0.98 0.88 1.22 1.00 0.9 1.13 250 L250K

250 L250M 0.90 1.09 1.13 1.20 1.0 1.05 250 L250N 0.22

250 L250P 0.25

0.07

250 L250Q 0.17

0.8 0.13 250 L250R 0.27

250 L250S 0.19

0.06

0.5 0.07 250 L250T 0.25 1.49 2.25 1.69 0.8 0.81 250 L250V 0.80 0.64 1.06 1.02 0.9 0.98 250 L250W 0.17

0.5 0.20 250 L250Y

251 E251A 0.93 0.92 0.67 0.98 0.6 0.70 251 E251C 0.66 0.99 1.04 1.14 0.8 0.69 251 E251D 0.76 1.08 1.07 1.12 0.8 0.95 251 E251F 0.68 0.96 0.65 1.04 0.7 0.66 251 E251G 0.65 1.07 0.83 1.17 0.6 0.95 251 E251H 0.64 1.03 0.74 1.04 0.5 0.74 251 E251I 0.58 0.93 0.91 0.93 0.5 0.81 251 E251K 0.62 0.54 0.41 0.89 0.1 0.65 251 E251L 0.60 0.85 0.54 1.04 0.7 0.72 251 E251M 0.65 0.78 0.62 0.87 0.6 0.62 251 E251N 0.69 0.96 0.78 1.09 0.6 0.85 251 E251P 0.20

1.05

251 E251Q 0.61 1.12 0.91 1.10 0.5 0.77 251 E251R 0.43 0.66 0.74 1.23 0.2 0.79 251 E251S 0.52 0.81 0.99 0.96 0.6 0.81 251 E251T 0.69 1.02 0.91 1.00 0.7 0.93 251 E251V 0.61 1.05 0.78 1.19 0.6 0.88 251 E251W 0.50 1.21 0.90 1.07 0.3 0.73 251 E251Y 0.58 0.92 0.57 0.97 0.4 0.74 252 N252A 1.02 1.03 1.28 0.97 1.0 0.93 252 N252C 1.01 0.91 0.88 1.01 1.1 0.83 252 N252D

252 N252E 0.77 0.94 0.93 1.01 1.1 0.95 252 N252F 0.27 1.07 0.77 1.10 0.9 0.49 252 N252G 0.88 1.23 0.86 1.08 1.1 0.97 252 N252H 0.94 1.17 0.88 1.09 1.1 0.97 252 N252I 0.81 1.07 1.11 0.94 1.0 1.10 252 N252K 1.08 0.87 0.86 0.93 1.0 0.90 252 N252L 0.96 1.09 0.85 1.08 1.0 1.02 252 N252M 0.89 0.98 1.11 1.10 1.1 1.03 252 N252P 0.18

252 N252Q 1.37 1.32 1.08 1.09 1.1 0.98 252 N252R 0.95 0.84 0.90 1.08 0.9 0.99 252 N252S 0.95 1.05 1.13 1.03 1.0 1.16 252 N252T 0.81 1.23 1.11 1.18 1.1 1.05 252 N252V 0.74 0.99 0.99 1.28 1.0 1.24 252 N252W 0.80 1.12 1.04 1.10 1.0 1.21 252 N252Y 0.82 1.06 0.93 1.14 1.0 1.09 253 T253A 1.02 0.94 1.16 0.98 0.9 0.82 253 T253C 0.81 0.89 1.19 0.95 1.0 0.86 253 T253D 0.77 1.10 1.02 1.03 0.8 0.78 253 T253E 0.91 1.10 1.08 0.92 1.0 0.87 253 T253F 1.00 1.10 0.88 1.01 1.0 0.82 253 T253G 0.97 0.97 1.04 1.05 0.8 0.86 253 T253H 1.25 0.99 0.94 1.04 1.0 0.89 253 T253I 0.43 1.14 0.91 0.90 0.1 0.66 253 T253K 0.94 0.89 0.83 1.09 0.6 0.88 253 T253L 0.86 1.15 0.85 1.08 0.8 1.00 253 T253M 1.04 0.88 1.05 1.19 0.8 0.84 253 T253N 0.92 1.10 1.14 1.03 1.0 0.88 253 T253P 0.18

0.2 0.10 253 T253Q 0.88 1.05 1.09 1.08 0.8 1.27 253 T253R 0.83 0.70 0.73 1.08 0.4 0.92 253 T253S 1.00 1.13 1.23 1.08 1.0 0.94 253 T253V 0.49 1.28 1.10 1.09 0.2 1.10 253 T253W

253 T253Y 0.21 3.47 2.00 1.61 0.2 0.10 254 T254A 1.14 0.93 1.13 1.00 1.0 0.76 254 T254C 1.01 0.99 1.08 1.14 1.1 0.83 254 T254D 0.26 2.25 1.81 1.66

0.53 254 T254E 0.25 1.23 1.03 1.06 0.1 0.39 254 T254F 0.17

0.11

254 T254G 0.55 1.00 1.16 1.13 0.8 0.85 254 T254H 0.16

0.46 254 T254I 0.48 1.08 1.07 1.16 0.2 0.81 254 T254K 0.21 0.88

0.60 0.1 0.22 254 T254L 0.37 1.14 1.00 1.33

0.61 254 T254M 0.27 1.06 0.92 1.30 0.1 0.34 254 T254N

254 T254P 0.83 1.16 0.97 1.07 0.7 0.88 254 T254Q 0.21 32.63  41.13  3.71

0.47 254 T254R 0.21 7.65 3.72 1.56

0.60 254 T254S 0.93 0.95 1.03 0.90 1.0 0.92 254 T254V 1.00 1.19 0.97 1.07 0.8 1.05 254 T254W 0.17

254 T254Y 0.18

0.14 255 T255A 1.09 0.98 0.97 0.96 #DIV/0! 0.85 255 T255C 1.06 1.04 1.12 0.95 #DIV/0! 0.89 255 T255D 0.96 1.13 1.10 0.99 #DIV/0! 0.91 255 T255E 1.00 1.12 0.97 1.08 #DIV/0! 0.97 255 T255F 0.84 1.12 1.12 0.93 #DIV/0! 1.27 255 T255G 0.90 1.06 1.10 1.04 #DIV/0! 0.99 255 T255H 0.87 1.12 1.03 1.04 #DIV/0! 0.97 255 T255I 0.99 1.27 0.98 1.13 #DIV/0! 1.02 255 T255K 1.00 0.86 0.91 1.06 #DIV/0! 1.11 255 T255L 0.96 1.52 1.00 0.95 #DIV/0! 1.02 255 T255M 1.04 0.93 1.13 0.92 #DIV/0! 1.02 255 T255N

255 T255P 0.24 1.56 0.99 1.35 #DIV/0! 0.38 255 T255Q

255 T255R 0.95 0.80 0.76 0.95 #DIV/0! 1.06 255 T255S 0.94 0.78 1.02 0.98 #DIV/0! 1.08 255 T255V 0.99 1.20 1.19 1.16 #DIV/0! 0.96 255 T255W 0.92 1.09 1.15 0.99 #DIV/0! 1.41 255 T255Y

256 K256A 1.00 1.06 1.22 0.97 #DIV/0! 0.96 256 K256C 0.97 0.94 1.00 0.89 #DIV/0! 1.10 256 K256D 0.90 1.22 1.24 0.95 #DIV/0! 0.96 256 K256E 0.99 1.15 1.06 0.88 #DIV/0! 0.94 256 K256F 0.96 0.95 1.21 0.96 #DIV/0! 0.98 256 K256G 0.72 1.30 0.91 1.03 #DIV/0! 1.00 256 K256H 1.04 1.20 1.20 1.03 #DIV/0! 1.03 256 K256I 0.93 1.18 1.22 1.03 #DIV/0! 1.03 256 K256L 0.97 1.21 1.12 0.92 #DIV/0! 1.04 256 K256M 0.94 1.17 1.29 1.10 #DIV/0! 1.12 256 K256N 0.90 1.12 1.15 0.94 #DIV/0! 1.09 256 K256P 0.91 1.10 1.09 1.00 #DIV/0! 1.35 256 K256Q 0.89 1.24 1.18 1.11 #DIV/0! 1.02 256 K256R 1.13 1.42 1.03 1.05 #DIV/0! 0.94 256 K256S 0.91 1.19 1.20 1.00 #DIV/0! 1.11 256 K256T 0.92 1.07 1.29 1.11 #DIV/0! 1.52 256 K256V 0.82 1.15 1.48 1.14 #DIV/0! 1.10 256 K256W 0.84 1.15 1.14 0.91 #DIV/0! 1.15 256 K256Y 0.44 1.23 1.27 1.02 #DIV/0! 1.02 257 L257A 0.72 1.00 1.27 0.91 0.6 0.99 257 L257C 0.78 1.09 1.04 1.05 0.8 0.83 257 L257D 0.37 1.17 1.22 0.83 0.4 0.68 257 L257E 0.50 1.05 1.27 0.92 0.6 0.81 257 L257F 0.67 0.60 1.05 0.91 0.2 0.98 257 L257G 0.67 1.01 0.64 1.20 0.7 0.90 257 L257H 0.56 0.83 1.00 1.01 0.4 0.87 257 L257I 0.83 0.89 1.04 0.97 0.9 1.06 257 L257K 0.59 0.62 0.75 0.85

0.90 257 L257M 0.84 1.06 0.93 0.86 0.8 0.83 257 L257N 0.52 1.16 1.00 1.00 0.5 0.87 257 L257P 0.45 0.69 0.96 0.91 0.3 0.73 257 L257Q

257 L257R 0.59 0.64 0.76 1.04 0.1 0.88 257 L257S 0.62 0.93 1.10 0.97 0.5 1.03 257 L257T 0.62 1.05 1.29 1.00 0.7 1.06 257 L257V 0.76 0.91 0.90 0.97 0.9 0.90 257 L257W 0.44 1.26 1.03 1.18

0.86 257 L257Y 0.62 1.17 1.00 0.98 0.4 0.84 258 G258A 0.59 1.05 1.13 1.14 0.1 0.61 258 G258C 0.53 0.87 1.15 1.03 0.4 0.62 258 G258E 0.57 0.98 1.11 1.12 0.9 0.71 258 G258F 0.48 0.99 1.09 1.05

0.75 258 G258H 0.50 1.00 1.07 1.09

0.68 258 G258I 0.29 1.26 1.39 1.41 0.3 0.53 258 G258K 0.50 0.99 0.92 1.15

0.82 258 G258L 0.50 0.89 1.10 1.14

0.72 258 G258M 0.43 1.02 1.05 1.29 0.1 0.63 258 G258P 0.31 1.41 1.63 1.56

0.65 258 G258Q 0.52 1.05 1.26 1.12 0.4 0.80 258 G258R 0.40 0.86 0.83 1.20

0.71 258 G258S 0.48 0.70 1.01 1.01

0.64 258 G258T

258 G258V 0.38 1.26 1.57 1.45 0.6 0.81 258 G258W 0.44 1.03 1.28 1.19

0.73 258 G258Y 0.46 1.08 1.13 1.33

0.79 259 D259A 0.94 0.61 0.43 0.93 #DIV/0! 1.03 259 D259C 1.04 0.84 0.98 0.90 #DIV/0! 1.02 259 D259E 0.99 1.15 0.97 0.98 #DIV/0! 1.05 259 D259F 0.77 0.54 0.41 0.66 #DIV/0! 1.09 259 D259G 0.91 0.58 0.58 0.94 #DIV/0! 1.07 259 D259H

259 D259I

259 D259K 1.16 0.31 0.46 0.72 #DIV/0! 1.08 259 D259L 0.98 0.52 0.51 0.69 #DIV/0! 1.04 259 D259M 0.91 0.50 0.53 0.78 #DIV/0! 1.07 259 D259N 1.02 0.60 0.75 1.08 #DIV/0! 1.19 259 D259P 0.87 0.61 0.74 0.83 #DIV/0! 1.11 259 D259Q 1.02 0.78 0.69 1.01 #DIV/0! 1.13 259 D259R 0.89 0.32 0.40 0.80 #DIV/0! 1.14 259 D259S 0.92 0.53 0.66 0.93 #DIV/0! 1.07 259 D259T 0.77 0.73 0.75 1.00 #DIV/0! 1.17 259 D259V 0.72 0.51 0.63 0.89 #DIV/0! 1.29 259 D259W 0.71 0.36 0.50 0.80 #DIV/0! 1.24 259 D259Y 0.66 0.42 0.48 0.73 #DIV/0! 1.28 260 S260A 1.06 0.95 1.29 0.98 #DIV/0! 0.91 260 S260C 0.99 1.11 1.13 0.82 #DIV/0! 1.05 260 S260D 0.94 1.22 1.05 0.90 #DIV/0! 0.92 260 S260E 1.03 1.11 1.10 0.97 #DIV/0! 0.88 260 S260F 0.89 0.91 1.17 0.99 #DIV/0! 0.93 260 S260G 0.97 1.21 1.11 1.12 #DIV/0! 1.27 260 S260H 1.17 0.97 1.10 0.95 #DIV/0! 1.08 260 S260I 0.48 1.13 1.16 1.15 #DIV/0! 0.98 260 S260K

260 S260L 0.92 1.22 1.00 1.16 #DIV/0! 1.05 260 S260M 0.99 1.06 1.07 1.05 #DIV/0! 0.97 260 S260N 0.94 1.13 1.20 1.14 #DIV/0! 1.06 260 S260P 1.02 1.19 1.07 0.99 #DIV/0! 1.14 260 S260Q

260 S260R 1.01 0.98 0.70 0.99 #DIV/0! 0.98 260 S260T 0.36 0.48 0.59 0.74 #DIV/0! 0.10 260 S260V 0.85 1.05 1.07 0.98 #DIV/0! 1.28 260 S260W 0.69 1.15 0.88 1.10 #DIV/0! 1.04 260 S260Y 0.86 1.28 0.92 1.07 #DIV/0! 1.20 261 F261A 0.55 0.82 0.95 0.91 0.5 0.59 261 F261C 0.57 0.80 1.08 0.95 0.7 0.68 261 F261D

261 F261E 0.65 0.65 1.05 0.94 0.7 0.68 261 F261G 0.46 0.75 0.82 0.80 0.2 0.55 261 F261H 0.74 0.92 1.04 0.99 0.8 0.77 261 F261I

261 F261K

261 F261L 0.77 0.84 0.77 0.95 0.8 0.62 261 F261M 0.73 0.79 0.90 0.76 0.7 0.73 261 F261N 0.80 0.92 0.88 0.92 0.8 0.72 261 F261P 0.45 0.87 0.86 0.95 0.3 0.60 261 F261Q 0.57 0.78 1.10 0.95 0.7 0.73 261 F261R 0.58 0.71 0.48 0.93 0.2 0.66 261 F261S 0.54 0.89 0.87 0.98 0.5 0.68 261 F261T 0.56 0.98 1.26 1.25 0.7 0.88 261 F261V 0.57 0.92 1.09 0.87 0.7 0.78 261 F261W 0.89 0.70 0.98 1.18 1.1 0.80 261 F261Y 0.67 0.63 0.94 0.97 0.9 0.79 262 Y262A 0.83 0.81 0.96 0.84 0.5 0.70 262 Y262C 1.10 0.91 0.98 0.83 0.9 0.78 262 Y262D 0.92 0.99 0.91 0.97 0.8 0.61 262 Y262E 0.86 1.01 1.11 1.06 0.9 0.77 262 Y262F 1.11 0.77 1.10 0.93 0.9 0.93 262 Y262G 0.55 0.94 0.60 1.03 0.2 0.56 262 Y262H 0.93 0.81 0.77 1.01 0.9 0.87 262 Y262I 0.72 0.59 0.86 0.90 0.6 0.53 262 Y262K 0.84 0.53 0.67 0.95 0.1 0.96 262 Y262L 0.92 0.96 1.06 0.90 0.9 0.81 262 Y262M 1.00 0.60 0.88 1.02 0.9 0.75 262 Y262N 0.82 1.00 1.13 0.86 0.7 0.77 262 Y262P 0.23 1.18 1.64 1.11

0.24 262 Y262Q 0.82 0.86 0.96 0.91 0.8 0.72 262 Y262R 0.78 0.39 0.62 0.83

0.76 262 Y262S 0.79 1.08 0.91 1.00 0.7 0.80 262 Y262T 0.65 0.94 0.95 0.86 0.7 0.71 262 Y262V 0.51 1.01 0.90 0.94 0.6 0.69 262 Y262W 0.83 0.81 0.99 1.03 0.8 0.89 263 Y263A 0.56 0.84 0.93 0.93 0.1 0.76 263 Y263C 0.98 0.86 0.98 0.93 0.6 0.90 263 Y263D 0.31 1.61 1.44 1.22 0.5 0.71 263 Y263E 0.47 1.02 0.98 0.86 0.5 0.80 263 Y263F 1.03 1.14 0.97 0.89 0.9 0.80 263 Y263G 0.32 0.59 1.09 0.83

0.41 263 Y263H

263 Y263I 0.27 1.10 1.16 1.17

0.41 263 Y263K 0.22 2.39 2.76 1.86 0.1 0.34 263 Y263L 0.84 0.89 0.83 0.95 0.2 1.00 263 Y263M 0.96 0.99 1.08 0.97 0.6 0.74 263 Y263N

263 Y263P 0.18

263 Y263Q

263 Y263R 0.21 8.02 4.08 1.72 0.1 0.26 263 Y263S 0.47 1.06 0.82 0.95 0.2 0.77 263 Y263T 0.91 0.84 0.97 1.10 0.7 0.97 263 Y263V 0.66 0.80 0.89 0.94 0.4 1.07 263 Y263W 0.35 0.96 0.90 0.95 0.1 0.64 264 G264A 0.55 0.81 0.96 0.93 0.3 0.79 264 G264C 0.25

0.10 0.13

264 G264D 0.20

1.31

264 G264E 0.19

0.30

264 G264F 0.28 0.08

264 G264H 0.19

264 G264I 0.43

264 G264K

264 G264L 0.26

0.09

264 G264M 0.20

0.85

264 G264N 0.18

0.3 0.08 264 G264P 0.18

0.07

264 G264Q 0.20

1.17

264 G264R 0.22 0.32 0.51 0.07

264 G264S 0.25 1.28 1.13 1.32

0.44 264 G264T 0.22

0.93 0.12

264 G264V 0.17

264 G264W 0.18

264 G264Y 0.17

265 K265A 1.18 1.03 1.24 0.86 0.8 0.96 265 K265C 0.92 0.96 1.54 1.11 0.9 0.93 265 K265D 0.59 1.05 1.24 0.85 0.9 0.77 265 K265E 0.70 1.00 1.32 0.90 1.0 0.94 265 K265F

265 K265G 0.89 1.22 1.38 1.04 0.7 0.97 265 K265H 0.69 1.16 1.06 0.92 1.1 0.88 265 K265I

265 K265L 0.59 1.11 1.44 1.11 1.2 0.97 265 K265M 0.78 1.04 1.19 0.99 1.0 0.88 265 K265N 1.05 1.07 1.31 1.00 1.2 0.85 265 K265P 0.25 1.61 1.92 1.59 1.0 0.80 265 K265Q 0.76 1.16 1.19 1.03 1.3 0.82 265 K265R 1.16 1.11 0.88 1.17 1.1 0.92 265 K265S 1.06 1.13 1.15 1.04 1.0 0.88 265 K265T 0.80 1.08 1.20 1.01 1.1 0.87 265 K265V 0.51 1.12 1.33 0.96 0.9 0.87 265 K265W 0.75 1.28 1.35 1.08 1.0 1.20 265 K265Y 0.85 1.07 1.25 1.02 1.0 1.26 266 G266A 0.23 0.16 0.07 0.18

266 G266C 0.21 0.22 2.27 0.36

266 G266D 0.31

266 G266E 0.26 0.09 0.06 0.07

266 G266F 0.26 0.08

0.08

266 G266H 0.19

20.22 

266 G266I

266 G266K

266 G266L 0.26

0.27 0.06

266 G266M 0.32

266 G266N 0.19

266 G266P 0.26

0.08

266 G266Q 0.18 0.08

266 G266R 0.22

0.12

266 G266S 0.24

0.11

266 G266T

266 G266V 0.22 0.51 0.33 0.16

266 G266W 0.18

266 G266Y 0.22 0.77 0.24 0.21

267 L267A 0.82 1.07 1.22 1.07 0.9 1.10 267 L267C 0.68 1.04 1.22 1.19 0.9 1.14 267 L267D 0.13

0.1 0.17 267 L267E 0.58 1.17 1.35 1.10 1.1 1.19 267 L267F 0.72 0.98 1.11 1.13 0.2 0.81 267 L267G 0.62 0.71 1.13 1.16 0.3 0.97 267 L267H 0.63 1.07 1.21 1.13 0.1 1.05 267 L267I 0.91 1.06 1.25 1.07 1.1 0.99 267 L267K 0.57 0.98 0.89 1.04

1.05 267 L267M 0.77 0.94 1.22 0.95 0.9 1.00 267 L267N 0.40 1.29 1.32 1.25

0.88 267 L267P 0.36 1.16 1.20 1.33

0.82 267 L267Q 0.73 1.14 1.32 1.11 0.9 1.27 267 L267R 0.53 0.96 0.91 1.06

0.95 267 L267S 0.71 1.03 1.07 1.16 0.5 1.15 267 L267T 0.63 1.19 1.25 1.33 0.5 1.33 267 L267V 0.73 1.12 1.08 1.24 0.8 1.06 267 L267Y 0.29 0.99 1.78 1.82

1.02 268 I268A 0.86 0.85 0.88 0.95 0.7 0.68 268 I268C 0.95 0.94 0.73 1.18 0.9 0.78 268 I268D

268 I268E 0.22 0.83 1.00 0.50 0.5 0.07 268 I268F 0.26 1.09 1.01 1.03

0.40 268 I268G 0.18

0.1 0.15 268 I268H 0.19 0.15

268 I268K 0.22 0.07 0.40 0.20

268 I268L 0.99 0.85 1.01 1.08 0.7 0.91 268 I268M 0.88 1.03 1.06 1.04 0.3 1.08 268 I268N 0.18

268 I268P 0.69 0.69 0.76 0.82 0.4 0.60 268 I268Q 0.25

0.26 0.23 0.2 0.08 268 I268R 0.25 0.12

0.08

268 I268S 0.30 1.40 1.31 1.55

0.80 268 I268T 0.25 1.90 1.96 1.76 0.8 0.44 268 I268V 0.93 0.95 0.76 1.13 1.0 0.90 268 I268W 0.21 2.80 2.43 0.16

268 I268Y

269 N269A 0.48 1.02 1.00 1.07 0.3 0.82 269 N269C

269 N269D 1.25 1.14 0.89 1.01 1.3 0.90 269 N269E 0.83 1.26 1.08 1.05 1.1 1.01 269 N269F 0.37 1.00 1.00 1.14

0.71 269 N269G 0.53 0.88 0.95 1.03 0.1 0.89 269 N269H

269 N269I 0.69 1.00 1.06 1.04 0.6 1.00 269 N269K 0.64 0.75 0.81 1.01 0.5 0.89 269 N269L 0.39 0.88 0.96 1.17 0.1 0.84 269 N269M 0.81 0.88 0.86 0.91 0.5 0.87 269 N269P 0.26

0.08 0.15

269 N269Q 0.84 1.00 0.85 1.19 1.0 0.96 269 N269R 0.46 0.63 0.63 0.98

0.72 269 N269S 0.94 1.02 1.15 1.12 0.8 1.00 269 N269T 0.56 0.85 0.91 0.91 0.3 0.88 269 N269V 0.44 1.01 0.97 1.24 0.5 0.95 269 N269W 0.20

14.66  0.1 0.41 269 N269Y

270 V270A 1.21 0.98 1.07 1.02 1.0 0.77 270 V270C 1.09 0.99 1.05 1.03 1.1 0.90 270 V270E 0.19

270 V270F 0.17 2.38 2.92 1.13 0.2 0.08 270 V270G 0.41 0.98 0.92 1.09 0.8 0.84 270 V270H 0.29

270 V270I 0.88 0.96 1.09 1.01 1.0 0.89 270 V270K 0.43

270 V270L 0.90 1.02 1.01 0.87 0.7 0.86 270 V270M 0.81 0.92 1.01 0.94 0.4 0.77 270 V270N 0.64 0.94 1.31 0.89 0.7 0.93 270 V270P 0.50 0.91 1.08 0.93 0.8 0.80 270 V270Q 0.20 0.31

270 V270R 0.51

270 V270S 1.08 0.99 0.95 0.78 1.0 0.84 270 V270T 0.94 0.96 1.07 1.01 0.8 1.06 270 V270W 0.23 0.11

270 V270Y 0.39

271 Q271A 1.18 0.94 1.12 1.04 1.1 0.83 271 Q271C 0.99 1.02 0.98 1.08 1.2 0.86 271 Q271D 1.00 1.03 0.84 1.00 1.1 0.89 271 Q271E 1.01 0.93 1.16 0.95 1.2 1.02 271 Q271F 1.09 1.04 0.80 1.05 1.0 0.89 271 Q271G 0.92 0.97 0.86 1.06 0.7 0.96 271 Q271H 0.92 1.01 0.85 1.09 1.0 1.04 271 Q271I 1.07 1.04 0.88 0.96 1.0 0.86 271 Q271K 1.03 0.60 0.57 1.09 0.5 1.01 271 Q271L 1.16 0.90 0.94 1.01 1.0 0.88 271 Q271M 1.15 0.89 1.19 1.11 1.0 0.96 271 Q271N 0.99 0.91 0.91 1.09 0.9 1.01 271 Q271P 1.03 0.75 1.12 1.06 1.1 0.76 271 Q271R 1.23 0.63 1.09 1.05 0.2 0.95 271 Q271S 0.97 0.85 1.02 0.98 1.0 0.96 271 Q271T 0.88 0.97 0.91 1.11 0.8 0.99 271 Q271V 0.92 1.06 0.84 1.11 0.9 0.97 271 Q271W 1.00 0.90 0.94 1.14 0.9 1.07 271 Q271Y 0.96 0.94 0.95 0.98 0.9 0.97 272 A272C

272 A272D

272 A272E 1.08 0.82 1.09 0.96 1.1 0.79 272 A272F 0.88 1.02 1.08 0.99 0.9 0.91 272 A272G 1.07 0.79 1.23 1.03 0.8 0.91 272 A272H 1.12 0.90 1.19 1.00 0.9 0.82 272 A272I 0.76 0.72 1.23 0.98 1.0 0.94 272 A272K 1.00 0.61 1.02 0.95 0.9 0.89 272 A272L 0.99 0.87 1.12 0.95 1.1 0.81 272 A272M 0.98 0.77 0.98 1.08 0.9 0.86 272 A272N

272 A272P 0.92 0.93 1.05 0.95 0.8 0.92 272 A272Q 1.19 0.86 1.18 1.02 1.0 0.88 272 A272R 0.99 0.47 0.99 0.81 0.8 1.00 272 A272S 1.00 1.04 1.19 1.09 1.0 0.97 272 A272T 0.88 0.97 0.99 1.04 1.0 1.19 272 A272V 0.80 1.01 1.14 0.99 1.0 1.00 272 A272W 0.91 0.52 1.04 1.07 0.9 1.21 272 A272Y 0.95 0.95 1.28 1.00 1.0 0.93 273 A273E 0.59 0.92 0.99 1.05 0.2 0.57 273 A273G 0.87 0.93 1.21 1.22 0.8 0.94 273 A273H 0.73 1.05 0.98 1.09 0.4 0.75 273 A273K 0.23 1.63 1.61 1.93

0.58 273 A273L 0.70 0.88 1.13 1.08 0.3 0.71 273 A273N 0.41 1.13 1.13 1.15 0.1 0.66 273 A273P 0.29 1.50 1.73 1.83

0.65 273 A273Q 0.44 1.09 1.19 1.42 0.1 0.75 273 A273R 0.24 1.43 1.20 2.03

0.63 273 A273S 0.87 1.06 1.35 1.15 0.7 0.98 273 A273T 0.53 0.79 1.23 1.29 0.2 0.91 273 A273V 0.53 1.41 1.24 1.15 0.3 0.84 273 A273W 0.26 2.08 1.97 1.53

0.81 274 A274C 0.94 1.10 0.99 0.96 1.0 0.97 274 A274D 0.94 0.92 0.87 0.89 0.7 1.05 274 A274E 0.45

274 A274F 0.80 0.82 0.84 0.96 0.6 0.74 274 A274G 0.85 0.94 0.88 0.92 0.9 0.96 274 A274H 0.79 1.17 0.89 0.95 0.5 0.98 274 A274I 0.98 0.99 0.92 1.07 1.0 1.03 274 A274K 0.54 0.94 0.61 0.95 0.2 0.76 274 A274L 0.78 1.21 0.92 1.03 1.1 0.83 274 A274M 0.84 0.87 0.72 0.98 1.0 0.72 274 A274N

274 A274P 0.54 0.99 0.70 1.02 0.4 0.63 274 A274Q 0.77 1.05 0.90 1.07 0.8 0.93 274 A274R 0.41 0.85 0.58 1.12 0.1 1.12 274 A274S 1.12 0.92 0.88 1.05 1.0 0.97 274 A274T 0.91 1.15 0.83 1.06 1.0 1.08 274 A274V 0.96 1.14 0.76 1.19 1.0 1.10 274 A274W 0.37 1.32 0.74 1.09 0.5 0.70 274 A274Y 0.57 1.06 0.86 1.05 0.6 0.93 275 Q275A 0.70 0.95 1.23 0.99 1.0 0.84 275 Q275C 0.41 1.04 1.23 0.91 1.1 0.83 275 Q275D 1.04 1.21 1.03 1.01 1.1 1.08 275 Q275E 1.17 1.01 1.20 1.23 1.1 0.95 275 Q275F 0.70 0.86 0.97 0.89 0.9 1.01 275 Q275G 0.90 0.90 0.81 1.05 1.1 0.77 275 Q275H 1.06 0.79 0.96 1.01 1.1 0.88 275 Q275I

275 Q275K 1.02 0.70 0.80 1.06 0.9 0.92 275 Q275L 0.86 0.78 1.01 0.97 1.0 1.00 275 Q275M 0.96 1.16 0.96 0.97 1.0 0.81 275 Q275N

275 Q275P 0.74 1.10 1.00 1.00 1.1 0.96 275 Q275R 1.05 0.81 0.80 1.03 0.9 0.97 275 Q275S 0.91 1.12 1.13 1.01 1.0 0.97 275 Q275T 0.85 1.06 1.01 1.05 1.0 0.98 275 Q275V 0.70 1.06 1.09 0.97 1.1 1.07 275 Q275W 0.96 1.02 1.08 1.20 1.0 1.09 275 Q275Y

Combinable Mutations:

Table 6-2 lists subtilisin BPN′ variants which are Combinable Mutations for the 275 positions (2,907). These variants have Performance index values >0.5 for at least one property, and >0.05 for both properties.

TABLE 6-2 Combinable Mutations of BPN′ PI BMI PI BMI PI BMI LAS- BPN′ TCA pH 8 pH 7 pH 8 EDTA AAPF Position variant PI 16 C. 16 C. 32 C. PI PI 1 A001C 0.74 0.84 1.10 0.79 1.1 0.87 1 A001D 1.34 0.93 1.12 0.88 1.1 0.88 1 A001E 0.82 0.94 0.85 0.84 1.5 0.94 1 A001F 1.39 0.94 1.01 0.84 0.4 0.90 1 A001G 1.39 0.90 1.12 1.06 1.1 1.04 1 A001H 1.26 0.99 1.04 0.98 0.9 0.97 1 A001I 1.50 0.72 1.00 0.92 0.6 0.88 1 A001K 1.23 0.83 0.79 1.11 0.2 0.96 1 A001L 0.96 0.86 0.81 0.94 0.6 0.94 1 A001M 1.34 1.02 1.07 1.08 0.9 0.99 1 A001N 1.29 1.02 0.81 0.98 1.0 1.05 1 A001P 0.27 1.16 1.46 1.14 0.7 0.66 1 A001Q 0.88 1.00 0.97 0.98 1.2 1.02 1 A001R 1.00 0.89 0.72 0.91 0.1 1.00 1 A001S 1.09 0.89 1.00 1.05 0.9 1.08 1 A001T 1.13 1.00 1.16 1.02 1.0 1.01 1 A001V 1.32 0.83 0.68 0.96 0.8 0.96 1 A001W 1.19 0.76 0.67 0.88 0.2 0.92 2 Q002C 0.55 0.81 1.26 0.92 0.1 0.74 3 S003A 1.19 1.20 0.97 0.89 0.3 0.93 3 S003D 1.24 1.11 1.08 0.97 1.0 1.02 3 S003F 1.20 0.90 0.95 0.86 0.2 1.02 3 S003I 1.24 0.80 0.90 1.05 1.0 0.92 3 S003K 1.28 0.97 0.80 0.95 0.1 1.09 3 S003L 1.13 0.90 0.84 1.06 0.6 0.92 3 S003M 1.35 0.83 1.04 0.92 1.1 0.84 3 S003N 1.18 0.98 1.15 0.85 0.5 1.01 3 S003Q 1.38 0.97 0.96 1.08 1.3 1.00 3 S003T 1.31 1.09 1.01 0.87 1.2 0.90 3 S003V 1.19 0.84 0.80 1.06 1.0 0.99 3 S003W 1.50 0.71 0.65 0.91 0.1 0.84 3 S003Y 1.25 0.76 0.72 0.92 0.2 0.88 4 V004C 0.87 1.03 1.22 0.92 0.3 1.09 4 V004E 1.00 1.04 1.22 0.92 0.1 0.99 4 V004T 1.02 0.92 1.27 0.97 1.2 1.20 5 P005F 0.22 0.55 0.44 0.61 0.1 0.23 5 P005G 0.98 1.09 1.10 0.98 0.3 1.13 5 P005I 0.21 0.49 0.96 1.02 0.1 0.20 5 P005K 0.16 4.53 2.60 0.65 0.6 0.06 6 Y006A 1.02 1.14 1.03 1.01 0.8 0.97 6 Y006C 1.04 1.03 0.95 0.83 0.7 0.91 6 Y006E 1.49 1.13 0.76 1.00 1.1 0.81 6 Y006F 1.17 0.84 0.88 0.81 0.6 0.92 6 Y006G 1.00 1.20 1.09 0.78 0.7 0.86 6 Y006M 1.31 1.16 1.04 0.96 0.6 0.86 6 Y006N 1.12 1.20 0.97 0.81 0.6 0.93 6 Y006P 0.92 1.10 0.77 0.96 0.7 1.13 6 Y006Q 1.36 1.29 1.19 0.87 0.9 0.94 6 Y006S 0.83 1.08 1.20 0.96 0.5 0.96 6 Y006T 1.13 1.02 1.14 1.12 0.7 0.85 6 Y006V 1.39 1.02 0.97 0.91 0.7 1.06 6 Y006W 1.96 1.06 1.00 0.96 1.1 0.82 7 G007C 0.20 0.75 0.37 1.11 0.2 0.08 7 G007T 0.19 2.98 2.43 3.02 0.1 0.21 8 V008C 0.81 0.87 0.93 1.10 0.1 0.83 8 V008I 0.91 1.06 0.87 1.01 1.0 0.93 8 V008K 0.19 3.07 3.04 3.06 0.2 0.45 8 V008L 0.83 0.91 0.98 1.03 0.2 0.80 8 V008R 0.21 0.83 0.14 1.14 0.2 0.06 9 S009A 1.22 0.84 1.00 0.98 0.8 0.97 9 S009C 1.32 0.94 0.80 0.79 1.2 1.15 9 S009E 1.89 0.91 0.76 0.92 1.5 0.91 9 S009G 1.19 0.88 0.92 0.88 0.7 0.91 9 S009H 1.35 0.70 1.08 1.00 0.8 0.95 9 S009L 1.30 0.99 0.76 0.86 0.6 1.05 9 S009M 1.32 0.98 0.95 0.99 0.8 1.17 9 S009P 1.38 1.00 0.87 0.94 0.7 1.06 9 S009Q 1.02 0.92 0.77 0.83 0.8 1.15 9 S009T 1.16 1.07 1.11 0.80 1.3 0.94 9 S009V 1.51 0.99 0.75 0.86 0.9 1.03 10 Q010A 1.06 0.90 1.06 1.00 0.5 0.87 10 Q010C 1.25 0.92 0.94 0.93 0.7 0.86 10 Q010E 1.07 0.70 1.01 0.99 1.5 0.79 10 Q010G 1.34 0.95 0.93 0.90 0.3 1.29 10 Q010H 1.20 1.04 1.07 0.92 0.9 1.29 10 Q010K 1.16 0.83 0.49 0.89 0.1 0.96 10 Q010M 1.26 0.82 0.97 1.07 0.5 0.90 10 Q010S 1.00 0.88 0.90 0.87 0.5 1.10 10 Q010T 1.25 1.04 1.00 0.85 0.8 0.93 10 Q010V 1.24 0.96 0.80 1.00 0.2 1.18 10 Q010Y 0.44 0.97 0.79 0.99 0.4 0.82 11 I011A 0.28 0.90 1.10 1.10 0.3 0.65 11 I011C 1.02 1.07 0.88 0.90 0.7 1.00 11 I011G 0.18 2.21 2.17 1.57 0.4 0.27 11 I011H 0.16 36.45 114.23 1.88 0.8 0.35 11 I011L 0.76 1.07 1.13 0.79 0.6 1.15 11 I011S 0.26 1.34 1.73 1.26 0.3 0.97 11 I011T 1.05 1.02 0.87 0.93 0.7 1.00 11 I011V 1.28 1.17 0.91 0.86 1.0 1.10 12 K012A 1.48 0.85 0.82 1.02 1.2 0.84 12 K012C 1.24 0.73 0.94 0.93 1.4 0.94 12 K012D 1.26 0.49 1.06 0.89 1.4 0.96 12 K012E 1.35 0.62 0.71 0.85 1.4 0.90 12 K012F 1.04 0.60 0.80 0.68 1.3 0.94 12 K012G 1.50 0.94 0.88 0.90 1.4 0.88 12 K012H 1.24 0.94 1.03 0.92 1.3 1.01 12 K012I 1.24 0.68 0.65 0.96 1.2 0.92 12 K012L 0.17 3.09 4.59 1.99 0.6 0.28 12 K012N 1.13 0.86 0.93 0.85 1.3 1.01 12 K012Q 1.35 0.96 0.61 1.01 1.3 1.10 12 K012R 0.73 0.83 0.84 0.83 0.9 0.75 12 K012S 1.07 0.71 0.74 0.72 1.0 0.93 12 K012T 1.13 1.07 0.95 0.84 1.1 0.85 12 K012V 1.57 0.80 0.83 0.98 1.1 0.76 12 K012W 1.35 0.54 0.85 0.94 1.2 0.90 12 K012Y 1.38 0.52 0.90 0.67 1.3 0.95 13 A013C 1.05 0.99 0.77 0.83 0.6 1.12 13 A013G 1.56 1.02 1.05 0.84 0.7 0.92 13 A013L 0.26 1.12 1.04 1.19 1.1 0.80 13 A013S 0.91 1.05 1.10 1.05 1.1 1.23 13 A013T 0.51 1.12 0.91 0.96 0.6 0.82 13 A013V 0.82 1.01 0.74 0.97 0.1 0.76 14 P014A 1.21 0.97 1.13 1.04 0.1 1.07 14 P014C 1.05 0.78 1.22 0.84 0.7 0.99 14 P014D 1.07 0.70 1.21 0.92 0.4 1.02 14 P014E 1.27 0.55 1.14 0.95 0.9 1.14 14 P014G 1.35 0.92 1.20 0.94 0.2 1.18 14 P014I 0.89 0.85 1.19 0.94 0.7 1.19 14 P014L 0.43 0.74 1.58 1.02 0.6 1.16 14 P014M 1.50 0.77 1.17 0.93 0.3 1.08 14 P014N 1.10 0.80 0.98 0.91 0.1 1.00 14 P014Q 1.34 0.62 0.94 0.81 0.6 1.12 14 P014S 0.96 0.79 1.06 0.96 0.1 1.13 14 P014T 0.98 0.99 1.08 0.83 0.9 1.35 14 P014V 1.32 0.88 1.10 0.90 0.7 1.12 15 A015C 1.72 0.83 0.87 0.90 1.3 0.83 15 A015D 1.60 0.66 0.77 0.75 1.3 1.00 15 A015E 1.68 0.62 0.77 1.11 1.5 0.87 15 A015F 1.39 0.78 0.68 0.85 0.9 0.99 15 A015G 1.63 0.77 0.66 0.76 0.9 0.79 15 A015H 0.90 0.64 0.77 0.93 1.0 1.01 15 A015I 1.52 0.46 0.88 0.86 1.1 0.95 15 A015K 1.50 0.74 0.59 0.69 0.3 0.98 15 A015L 1.52 0.89 0.77 0.88 1.1 0.85 15 A015M 0.96 0.95 0.62 1.01 1.0 0.99 15 A015P 1.41 0.57 0.64 0.73 0.9 0.95 15 A015Q 1.39 0.55 0.73 1.05 1.1 1.06 15 A015R 1.44 0.67 0.53 0.84 0.1 0.95 15 A015S 1.17 0.74 0.80 1.07 0.9 1.08 15 A015T 1.53 0.85 0.68 0.93 1.0 1.00 15 A015V 1.50 0.77 0.73 0.89 1.0 0.93 15 A015W 0.45 0.59 0.88 1.18 0.8 0.93 15 A015Y 1.43 0.63 0.70 0.90 1.0 0.94 16 L016A 1.14 0.79 1.22 0.96 0.8 0.84 16 L016C 1.01 0.71 1.15 1.08 1.0 1.13 16 L016E 1.02 0.57 1.18 1.09 0.9 1.03 16 L016F 0.45 0.63 0.93 0.89 0.5 0.58 16 L016G 0.29 0.54 1.19 0.97 0.8 0.47 16 L016H 0.29 0.70 1.11 1.12 0.5 0.53 16 L016I 1.22 0.51 1.21 1.05 1.0 0.89 16 L016K 0.36 0.62 1.09 0.99 0.5 0.73 16 L016M 1.63 0.76 0.97 1.13 1.0 0.89 16 L016N 0.59 0.71 1.10 1.05 0.8 0.96 16 L016P 0.50 0.73 1.05 1.07 0.8 0.90 16 L016Q 0.90 0.88 1.02 1.04 0.9 0.88 16 L016S 0.92 0.81 1.09 0.96 0.7 0.82 16 L016T 1.30 0.63 1.02 1.07 0.9 0.93 16 L016W 0.17 3.37 6.22 3.16 0.1 0.35 17 H017A 0.37 0.41 0.95 0.94 0.4 0.40 17 H017C 0.33 0.80 0.73 1.01 0.7 0.39 17 H017E 0.30 0.81 1.09 1.00 0.4 0.63 17 H017F 1.40 0.72 1.01 0.85 0.3 0.86 17 H017G 0.19 1.02 0.45 1.57 0.6 0.25 17 H017I 1.36 0.57 0.99 1.10 0.8 0.94 17 H017L 1.15 0.90 1.06 0.93 0.5 0.82 17 H017M 1.29 0.60 1.24 0.94 0.7 0.84 17 H017S 0.20 1.15 1.18 1.54 0.4 0.34 17 H017T 0.47 0.97 1.25 1.13 0.2 0.89 17 H017V 0.80 0.67 0.96 1.02 0.4 0.67 18 S018A 0.89 0.57 1.16 0.91 0.9 0.95 18 S018D 1.72 0.78 1.03 0.86 0.8 0.86 18 S018E 1.65 0.75 1.15 0.99 1.3 0.85 18 S018F 1.74 0.80 1.14 0.95 0.4 0.87 18 S018G 1.37 0.80 0.96 1.04 1.0 0.85 18 S018H 1.72 0.83 1.07 1.05 1.0 0.93 18 S018I 1.89 0.66 1.33 0.90 0.6 0.88 18 S018K 1.75 0.63 1.14 0.94 0.1 0.99 18 S018L 1.48 0.73 1.25 0.96 0.7 0.96 18 S018M 1.72 0.93 1.28 1.04 0.9 0.91 18 S018N 1.68 0.59 1.12 0.94 1.1 0.91 18 S018P 1.19 0.65 1.06 0.83 1.3 0.75 18 S018Q 1.68 0.80 1.12 0.99 1.0 0.92 18 S018T 1.64 0.67 1.25 0.99 1.1 0.89 18 S018V 1.67 0.57 1.17 1.14 0.8 0.89 18 S018W 1.59 0.73 1.06 1.00 0.4 0.95 18 S018Y 1.86 0.81 1.25 1.08 0.8 1.13 19 Q019A 1.82 1.07 0.99 1.05 0.8 0.92 19 Q019C 0.88 1.08 0.90 0.81 1.0 0.91 19 Q019D 0.87 0.98 0.95 0.67 1.1 0.98 19 Q019E 1.02 0.97 0.61 0.90 1.2 0.95 19 Q019G 1.33 0.99 1.15 0.87 0.8 1.13 19 Q019H 0.82 1.05 0.98 0.72 0.9 1.08 19 Q019I 0.89 1.06 0.87 1.03 0.9 1.22 19 Q019K 0.86 0.87 0.78 0.77 0.6 1.15 19 Q019L 0.98 0.95 0.61 0.87 1.0 1.01 19 Q019M 0.90 1.02 1.01 0.90 0.7 0.96 19 Q019R 1.09 1.03 0.64 0.74 0.4 0.99 19 Q019S 0.82 1.03 1.14 0.92 0.8 1.07 19 Q019T 0.93 0.94 1.00 0.84 0.8 1.15 19 Q019V 0.88 1.12 1.04 0.97 0.7 1.22 20 G020A 1.12 0.90 0.99 0.93 0.8 0.80 20 G020C 0.96 0.81 1.12 0.99 1.0 0.95 20 G020D 1.00 0.82 1.19 1.02 1.1 0.99 20 G020E 1.27 0.91 1.04 1.01 1.0 1.01 20 G020F 0.88 0.64 1.15 1.06 1.0 0.84 20 G020H 1.00 0.66 1.20 1.08 1.0 0.92 20 G020I 0.22 0.44 1.36 1.12 0.9 0.34 20 G020K 0.90 0.70 0.95 0.93 0.4 1.06 20 G020L 0.75 0.74 1.14 0.89 1.0 0.92 20 G020M 0.98 0.83 1.08 0.97 0.9 0.89 20 G020N 0.96 0.91 1.18 0.90 1.0 1.03 20 G020P 0.26 0.63 1.11 0.98 0.9 0.49 20 G020Q 0.95 0.53 1.13 1.01 0.9 1.06 20 G020R 0.86 0.70 0.99 0.92 0.2 0.99 20 G020S 1.00 0.63 1.07 1.05 0.7 0.88 20 G020T 0.54 0.82 1.24 1.08 0.9 1.02 20 G020V 0.22 0.97 1.37 1.53 0.8 0.40 20 G020W 0.63 0.88 1.15 1.05 0.8 0.93 20 G020Y 0.70 0.57 1.03 1.04 0.9 0.92 21 Y021A 1.15 0.85 0.77 0.94 0.9 0.81 21 Y021C 1.15 0.79 1.02 0.86 0.9 1.05 21 Y021D 0.84 0.83 0.76 1.02 0.9 0.73 21 Y021E 0.71 0.82 0.77 0.89 1.0 0.91 21 Y021F 1.13 0.59 0.77 0.97 1.0 0.85 21 Y021G 0.46 0.60 0.76 0.89 1.0 0.52 21 Y021H 1.22 0.78 0.69 0.98 1.1 0.93 21 Y021K 0.72 0.61 0.47 1.00 0.8 0.91 21 Y021L 0.92 0.78 0.75 0.99 1.0 0.95 21 Y021M 1.17 0.88 0.87 0.95 1.0 0.78 21 Y021P 0.47 0.50 0.88 1.08 1.2 0.69 21 Y021Q 0.74 0.88 0.87 1.02 0.9 0.96 21 Y021R 0.95 0.70 0.77 0.94 0.7 0.91 21 Y021S 0.98 0.71 0.84 0.93 0.9 0.80 21 Y021T 1.33 0.81 0.76 0.93 1.0 0.90 21 Y021V 1.15 0.70 0.99 1.00 1.1 0.87 21 Y021W 0.83 0.68 0.70 1.04 1.0 1.14 22 T022A 0.67 0.85 0.92 0.86 1.2 0.80 22 T022C 1.21 1.12 0.74 1.08 1.3 1.13 22 T022D 0.76 0.98 0.74 1.03 1.3 0.97 22 T022E 1.33 1.01 0.89 0.90 1.6 1.04 22 T022F 1.37 1.09 0.73 1.06 1.2 0.90 22 T022G 1.60 1.00 0.92 1.02 1.2 0.87 22 T022H 1.17 1.09 0.88 1.14 1.1 0.99 22 T022I 1.26 1.17 0.91 1.28 1.0 1.08 22 T022K 1.19 0.78 0.73 1.02 0.4 1.25 22 T022L 0.92 0.90 0.73 1.07 0.9 0.92 22 T022M 1.34 0.92 0.85 1.07 1.0 1.13 22 T022N 1.13 0.90 0.95 1.03 1.2 1.07 22 T022P 0.58 0.78 0.62 0.89 1.3 0.52 22 T022Q 1.42 1.15 0.75 1.14 1.1 0.97 22 T022S 1.10 0.95 0.91 0.98 1.3 0.93 22 T022V 1.32 1.18 0.75 1.10 1.3 1.11 22 T022W 1.52 0.93 0.79 1.07 1.7 0.87 22 T022Y 1.15 0.96 0.95 1.03 1.4 0.95 23 G023A 0.63 1.05 0.84 1.02 1.0 0.79 23 G023S 0.17 10.83 4.09 2.61 1.1 0.13 24 S024C 1.12 1.15 0.86 0.94 1.1 0.97 24 S024F 1.07 1.15 0.93 1.05 1.0 1.22 24 S024G 0.56 0.92 0.68 1.01 1.2 0.68 24 S024H 0.97 1.11 0.98 1.18 1.1 1.28 24 S024I 1.02 1.16 1.02 1.15 1.1 0.98 24 S024K 1.17 1.03 0.82 1.04 0.9 0.97 24 S024L 1.17 1.02 1.01 1.02 1.2 1.16 24 S024M 1.15 1.07 0.98 1.02 1.2 0.88 24 S024N 1.16 0.99 0.88 1.11 1.2 1.01 24 S024P 0.44 1.10 0.76 0.96 1.1 0.72 24 S024Q 0.90 0.96 0.94 1.11 1.0 1.10 24 S024R 0.86 1.19 0.82 1.12 1.0 1.19 24 S024T 0.57 1.07 0.92 1.06 1.1 0.96 24 S024V 0.45 1.21 0.93 1.19 1.1 1.22 24 S024W 1.13 1.09 0.62 1.09 1.2 0.94 24 S024Y 1.06 0.95 0.83 0.96 1.1 1.19 25 N025A 0.73 0.63 1.09 1.00 0.9 0.93 25 N025E 1.31 0.61 1.16 1.03 1.2 1.13 25 N025F 1.09 0.69 1.14 1.12 1.1 0.97 25 N025G 1.21 0.65 1.20 0.99 1.0 1.05 25 N025H 1.16 0.57 1.06 1.07 1.1 0.98 25 N025I 0.95 0.72 1.29 0.83 1.0 1.00 25 N025K 0.96 0.64 1.04 0.96 1.0 0.99 25 N025L 0.64 0.62 1.02 1.09 1.1 0.98 25 N025M 1.31 0.82 1.18 1.04 1.0 1.01 25 N025P 0.71 0.53 1.10 0.81 0.8 0.82 25 N025Q 1.10 0.61 1.21 1.09 1.0 1.08 25 N025R 1.34 0.68 1.02 1.12 1.0 1.03 25 N025S 0.85 0.60 1.18 1.01 1.0 0.93 25 N025T 1.06 0.73 1.21 1.12 0.8 1.22 25 N025V 0.59 0.45 1.27 1.11 0.9 1.01 25 N025W 1.42 0.53 1.30 1.00 0.9 0.99 26 V026C 1.14 0.96 0.91 1.02 1.0 0.88 26 V026E 0.36 1.12 0.79 1.19 1.0 0.87 26 V026F 0.35 0.97 0.90 1.19 1.1 0.68 26 V026G 0.54 0.91 0.75 1.07 1.0 0.82 26 V026H 0.46 1.45 0.86 1.19 1.1 0.89 26 V026I 0.91 0.75 0.70 1.09 1.2 0.90 26 V026K 0.77 1.03 0.67 1.11 1.1 0.95 26 V026L 0.59 0.92 0.85 0.96 1.0 1.03 26 V026M 0.80 0.90 0.85 0.98 1.0 0.90 26 V026N 0.44 1.00 0.79 1.21 1.0 0.96 26 V026Q 0.61 0.96 0.78 1.02 1.0 1.08 26 V026S 0.82 0.82 0.85 0.95 0.9 0.86 26 V026T 0.92 0.98 0.98 1.02 0.9 1.04 26 V026W 0.25 2.33 1.16 2.13 1.1 0.95 26 V026Y 0.31 1.34 1.28 1.50 1.0 0.98 27 K027A 1.08 0.76 1.13 1.05 1.0 1.07 27 K027D 1.15 0.72 1.10 1.00 1.1 0.93 27 K027E 0.45 0.93 1.11 1.09 1.0 1.06 27 K027F 0.25 0.76 1.59 1.33 1.1 0.58 27 K027G 0.76 0.65 1.27 0.95 1.0 1.15 27 K027H 1.03 0.72 1.19 0.99 1.1 1.10 27 K027I 0.18 0.49 1.78 0.91 1.4 0.20 27 K027L 0.76 0.72 1.29 0.87 1.1 0.89 27 K027M 0.64 0.71 1.31 0.91 1.0 1.06 27 K027P 0.18 1.31 3.37 2.05 1.1 0.46 27 K027R 1.09 0.64 1.16 0.96 1.0 1.19 27 K027S 0.93 0.92 1.11 1.04 1.0 1.11 27 K027T 0.56 0.85 1.39 1.09 1.0 1.09 27 K027W 0.36 0.69 1.47 1.33 0.9 0.93 27 K027Y 0.45 1.00 1.19 1.03 0.9 0.96 28 V028A 0.46 0.95 0.84 1.02 0.9 0.72 28 V028C 0.65 1.20 0.99 1.08 1.0 0.94 28 V028H 0.20 1.08 0.79 1.03 1.1 0.22 28 V028I 1.02 1.27 1.00 1.06 1.1 0.87 28 V028M 1.05 0.99 0.68 0.91 0.6 0.70 28 V028N 0.21 0.31 0.67 0.50 1.1 0.13 28 V028Q 0.18 2.79 1.99 1.43 1.6 0.25 28 V028S 0.18 5.70 5.17 3.40 1.1 0.37 28 V028T 0.58 1.31 1.18 1.13 1.0 1.21 29 A029C 0.76 1.32 1.19 1.13 0.9 0.77 29 A029D 0.19 2.95 2.74 2.34 0.9 0.42 29 A029G 0.94 1.08 0.88 1.06 1.0 1.11 29 A029S 0.47 1.64 1.13 1.23 1.1 1.01 29 A029T 0.24 2.02 1.55 1.57 1.1 0.47 29 A029V 0.38 1.85 1.52 1.62 1.0 0.83 30 V030A 0.38 0.98 1.04 0.87 0.9 0.41 30 V030C 0.91 0.83 0.85 0.99 1.0 0.37 30 V030D 0.20 2.34 2.31 1.96 0.9 0.22 30 V030E 0.17 30.23 33.27 4.25 0.8 0.15 30 V030I 1.15 1.16 1.03 1.07 1.1 0.82 30 V030L 1.24 1.09 0.86 0.87 1.0 0.24 30 V030M 0.89 0.66 0.80 0.79 0.8 0.11 30 V030N 0.25 1.06 1.30 1.50 1.1 0.15 30 V030S 0.28 1.25 1.21 1.43 0.3 0.12 30 V030T 0.30 1.39 1.27 1.38 0.9 0.37 31 I031A 0.90 0.96 0.85 0.97 1.1 1.64 31 I031C 0.94 1.16 0.87 1.02 1.1 1.53 31 I031D 0.20 1.18 1.43 1.13 1.2 0.28 31 I031E 0.21 2.56 1.98 2.40 1.1 1.12 31 I031F 0.92 1.26 0.92 1.00 1.1 1.89 31 I031G 0.17 5.42 3.74 2.40 1.1 0.40 31 I031H 0.26 1.98 1.57 1.79 1.3 1.22 31 I031K 0.32 1.84 1.28 1.39 1.2 1.03 31 I031L 1.12 0.89 0.88 0.85 1.2 1.70 31 I031M 1.21 0.98 0.83 0.99 1.1 1.60 31 I031N 0.23 2.34 2.01 1.96 1.3 0.74 31 I031P 0.24 0.16 0.06 0.17 1.5 0.09 31 I031Q 0.19 5.38 3.51 3.08 1.1 0.64 31 I031S 0.21 3.71 2.83 2.91 1.1 0.86 31 I031T 0.38 1.21 1.04 0.91 1.1 1.17 31 I031V 0.83 1.03 1.09 1.03 0.9 1.20 31 I031Y 0.21 4.14 3.02 3.08 0.9 0.90 33 S033A 0.82 0.84 0.84 0.83 0.7 0.29 33 S033C 0.73 0.66 0.55 0.71 1.0 0.19 33 S033E 0.44 1.21 0.81 0.92 0.8 0.07 33 S033G 0.96 1.14 0.80 1.01 0.9 0.17 33 S033N 0.45 1.14 0.90 1.03 0.6 0.38 33 S033Q 0.36 0.69 0.72 0.72 0.5 0.13 33 S033T 0.82 0.74 0.64 0.85 1.0 1.40 33 S033V 0.50 0.56 0.57 0.54 0.9 0.09 34 G034A 0.27 0.81 0.91 0.81 0.5 0.09 35 I035A 0.59 0.82 1.14 0.92 0.9 0.69 35 I035C 0.95 0.65 1.41 1.06 1.0 0.95 35 I035G 0.18 0.21 1.85 1.07 1.0 0.16 35 I035L 0.61 0.68 1.14 1.03 0.7 0.74 35 I035M 0.33 0.71 1.27 1.07 0.8 0.59 35 I035S 0.24 1.04 2.03 1.68 0.7 0.96 35 I035T 0.42 0.89 1.31 1.15 0.8 1.40 35 I035V 0.83 0.85 1.17 1.03 0.9 1.13 36 D036A 1.00 0.58 0.60 0.94 0.4 0.78 36 D036C 0.98 0.91 0.75 0.87 0.3 0.71 36 D036E 1.30 1.13 0.83 0.94 0.6 0.91 36 D036H 0.56 0.49 0.52 1.00 0.6 0.95 36 D036Q 0.67 0.62 0.54 0.99 0.9 0.98 36 D036S 1.03 0.72 0.70 0.87 0.1 0.93 36 D036T 0.72 0.64 0.45 0.87 0.1 0.85 37 S037A 1.25 1.14 1.07 0.73 0.9 1.03 37 S037C 1.09 0.90 0.87 0.93 1.0 0.94 37 S037E 0.72 0.83 1.06 0.84 1.0 0.92 37 S037F 0.99 1.05 0.88 0.91 1.0 0.83 37 S037G 1.21 1.19 0.95 0.95 1.0 1.25 37 S037H 1.04 1.06 0.98 0.90 0.9 1.04 37 S037K 1.31 0.98 0.63 0.84 1.1 1.02 37 S037L 0.98 1.04 0.91 0.78 0.8 0.87 37 S037M 1.31 1.00 1.07 0.82 0.9 0.87 37 S037P 0.48 1.48 0.90 1.13 0.4 0.70 37 S037Q 1.31 1.09 1.24 0.87 0.9 1.05 37 S037R 1.26 0.98 0.63 0.85 1.2 1.05 37 S037T 0.94 1.05 1.00 0.87 0.7 0.95 37 S037V 0.98 1.09 0.86 0.76 0.7 1.39 37 S037W 1.07 1.01 1.01 0.88 0.8 0.86 38 S038A 1.17 1.14 1.06 1.03 0.9 0.90 38 S038C 1.27 0.96 1.02 1.03 1.2 0.82 38 S038D 0.67 1.26 1.19 1.07 1.2 0.97 38 S038E 1.31 1.02 1.11 0.97 1.3 0.84 38 S038F 0.97 0.99 0.97 1.07 1.0 1.22 38 S038G 1.43 1.01 1.04 1.13 0.9 0.97 38 S038I 1.07 0.98 1.08 1.01 1.1 0.89 38 S038K 1.25 0.75 0.80 1.02 1.3 0.93 38 S038L 1.06 0.90 1.11 1.12 1.1 1.02 38 S038M 1.33 1.10 1.07 1.00 1.0 0.91 38 S038P 1.16 1.12 0.93 0.99 0.5 0.76 38 S038Q 1.11 1.06 0.87 1.08 1.1 0.96 38 S038R 2.01 0.65 0.89 1.01 1.4 0.89 38 S038T 1.20 0.86 1.07 1.05 1.1 0.93 38 S038V 1.28 1.05 1.07 1.02 1.1 1.02 38 S038W 1.15 0.75 0.77 1.04 1.3 0.91 39 H039Q 1.07 0.90 0.95 0.93 0.4 1.19 40 P040A 1.01 1.23 1.09 1.08 0.8 1.22 40 P040C 0.99 1.04 1.19 1.15 1.1 1.12 40 P040E 1.21 1.05 1.34 1.05 1.6 1.01 40 P040F 0.92 1.12 1.21 1.09 0.9 1.02 40 P040G 1.06 1.04 1.11 1.14 0.1 1.11 40 P040H 0.89 0.97 0.98 1.17 0.5 1.09 40 P040I 0.83 1.12 1.30 1.10 0.7 1.23 40 P040L 1.06 1.20 1.05 1.10 1.0 1.09 40 P040M 1.01 1.07 1.24 1.10 0.6 0.98 40 P040N 0.88 1.12 1.14 1.07 0.5 1.18 40 P040Q 1.01 1.16 1.13 1.11 1.1 1.01 40 P040S 0.84 1.15 1.06 0.81 0.3 1.12 40 P040T 0.81 1.29 1.68 1.22 0.1 1.20 40 P040V 0.91 1.04 1.07 1.09 0.7 1.06 40 P040W 1.09 0.87 0.90 1.13 1.0 1.12 40 P040Y 0.89 1.07 1.07 1.06 0.5 1.02 41 D041S 0.23 3.12 1.52 1.20 0.5 0.33 42 L042C 0.41 0.71 0.95 1.06 0.2 1.08 42 L042H 0.23 0.98 1.26 1.11 0.3 0.38 42 L042I 1.15 0.87 0.56 0.92 0.8 0.77 42 L042M 0.80 1.20 0.99 1.00 0.7 0.92 42 L042N 0.23 0.80 0.86 1.21 0.6 0.48 42 L042V 0.97 0.96 0.88 0.98 0.5 0.82 43 K043A 0.87 0.67 1.08 0.90 1.2 1.01 43 K043C 0.83 0.60 1.17 0.89 1.4 0.99 43 K043D 0.88 0.70 1.16 0.71 1.3 1.03 43 K043E 0.80 0.56 1.04 0.74 1.3 1.13 43 K043F 0.74 0.72 1.24 0.78 1.3 1.02 43 K043G 0.96 0.88 0.82 0.93 1.3 1.06 43 K043I 0.72 0.57 1.12 0.95 0.7 1.17 43 K043L 0.96 0.58 0.88 0.84 1.3 0.88 43 K043M 1.02 0.79 1.19 0.97 1.1 1.07 43 K043N 0.80 0.85 1.31 0.81 1.2 1.32 43 K043Q 0.95 0.61 1.09 0.90 1.3 1.05 43 K043R 1.14 0.56 1.30 0.87 0.9 1.33 43 K043S 0.98 0.77 1.14 0.92 1.3 0.99 43 K043T 0.93 0.92 1.06 0.96 1.1 1.07 43 K043V 1.10 0.59 0.98 0.93 0.6 1.26 43 K043W 0.85 0.67 0.98 0.90 1.3 1.03 43 K043Y 0.87 0.67 1.12 0.82 1.1 1.60 44 V044A 0.71 0.91 1.16 1.01 0.7 0.81 44 V044C 0.93 0.94 1.26 0.79 0.8 0.90 44 V044E 0.18 0.71 2.18 1.98 0.5 0.19 44 V044G 0.21 0.75 1.66 1.12 0.5 0.34 44 V044H 0.19 1.63 2.57 1.57 0.5 0.38 44 V044I 0.92 0.76 0.98 1.07 0.9 1.08 44 V044L 0.85 0.67 1.03 0.85 0.8 0.88 44 V044M 0.65 0.95 1.33 1.03 0.6 0.82 44 V044P 0.67 0.83 1.25 1.03 0.4 0.78 44 V044Q 0.20 1.48 2.85 1.49 0.6 0.33 44 V044R 0.19 0.79 1.62 0.69 0.2 0.13 44 V044S 0.33 1.03 1.51 1.13 0.5 0.86 44 V044T 0.30 1.32 1.94 1.30 0.7 1.26 44 V044Y 0.62 0.79 1.22 1.13 0.7 1.04 45 A045C 1.09 0.89 0.76 0.89 1.2 1.05 45 A045E 1.06 1.10 0.97 0.82 1.2 1.07 45 A045F 1.04 0.88 0.81 1.00 1.0 1.11 45 A045H 1.04 0.86 0.76 0.91 1.1 1.11 45 A045I 1.07 1.08 0.81 1.16 1.2 1.03 45 A045K 1.05 1.00 0.69 1.06 0.9 1.03 45 A045L 1.03 0.72 0.82 0.99 1.0 1.19 45 A045M 1.15 1.02 0.87 1.00 1.2 1.09 45 A045N 1.35 1.03 0.91 0.88 1.1 1.03 45 A045P 0.87 0.82 0.90 0.96 0.7 1.20 45 A045Q 1.07 0.84 0.95 1.09 1.1 1.16 45 A045S 1.08 0.93 0.87 0.86 1.2 1.02 45 A045T 0.99 1.04 1.31 0.90 1.2 1.01 45 A045V 1.28 0.85 0.81 1.03 1.1 1.12 45 A045Y 1.03 0.81 0.67 0.73 1.1 1.13 46 G046A 0.92 1.09 0.97 1.00 1.0 0.90 46 G046C 0.39 1.28 0.81 0.90 1.1 0.82 46 G046E 0.57 1.10 0.70 0.95 1.0 1.16 46 G046F 0.39 1.40 0.95 1.03 1.0 0.88 46 G046H 0.48 0.98 0.99 1.25 1.0 1.20 46 G046K 0.44 0.88 0.72 1.09 0.8 1.20 46 G046L 0.27 1.57 1.44 1.42 0.8 0.78 46 G046M 0.42 1.30 0.84 1.14 0.9 0.96 46 G046N 0.69 0.79 0.72 1.05 1.1 0.94 46 G046S 0.74 0.86 0.78 0.94 0.9 1.16 46 G046T 0.39 1.21 0.96 0.79 0.8 1.04 46 G046V 0.23 4.92 3.26 2.09 0.8 0.74 46 G046W 0.44 1.08 0.66 0.90 1.0 1.13 46 G046Y 0.36 1.02 1.27 1.12 0.8 1.23 47 G047A 0.32 0.98 0.96 1.04 0.5 0.30 47 G047C 0.24 0.64 1.09 0.88 0.6 0.15 47 G047E 0.23 0.72 0.99 1.02 0.6 0.14 47 G047F 0.25 0.96 0.86 1.15 0.5 0.15 47 G047H 0.23 1.04 1.17 1.20 1.1 0.47 47 G047M 0.22 0.63 0.89 0.87 0.5 0.10 47 G047S 0.21 1.19 1.04 1.24 0.5 0.15 47 G047T 0.17 4.45 4.77 2.27 0.5 0.12 47 G047W 0.18 2.60 2.43 2.22 0.5 0.17 48 A048C 1.15 1.14 1.16 0.85 1.1 0.95 48 A048D 1.13 1.01 1.00 0.97 1.1 0.89 48 A048E 1.17 0.84 0.93 1.02 1.2 0.90 48 A048F 1.08 1.08 0.92 0.96 1.0 0.89 48 A048H 1.08 0.87 1.16 1.04 1.1 0.87 48 A048I 1.02 0.79 0.91 1.02 1.2 1.00 48 A048K 1.13 0.90 0.55 0.91 1.1 0.90 48 A048L 0.99 0.87 0.97 0.99 1.0 0.91 48 A048M 0.59 1.21 0.99 0.87 1.1 0.92 48 A048Q 1.10 0.83 0.69 1.03 1.0 1.02 48 A048R 1.11 0.83 0.51 0.98 0.9 1.05 48 A048S 0.98 1.08 0.47 1.06 1.0 1.03 48 A048T 0.98 1.06 0.77 0.84 1.1 0.97 48 A048V 1.47 0.99 0.61 0.92 1.0 0.94 48 A048W 0.81 0.69 0.74 0.81 0.9 1.04 48 A048Y 1.03 0.84 0.81 0.86 1.0 0.90 49 S049A 0.35 0.54 0.61 1.02 0.9 0.30 49 S049C 0.61 0.48 0.69 0.97 0.5 0.38 49 S049D 0.23 1.09 1.53 1.69 0.5 0.36 49 S049G 0.28 0.78 0.75 1.64 1.2 0.50 49 S049I 0.18 2.22 2.52 2.14 0.5 0.11 49 S049N 0.35 1.04 0.88 1.32 0.5 0.64 49 S049T 0.29 0.95 1.23 1.37 0.5 0.46 49 S049V 0.21 1.58 1.39 2.10 0.4 0.30 50 M050A 0.78 1.16 0.85 0.89 0.9 1.09 50 M050C 0.89 1.17 0.89 0.80 1.1 1.01 50 M050D 0.17 6.35 0.87 0.90 1.0 0.16 50 M050F 0.95 1.01 0.96 0.81 1.1 1.09 50 M050H 0.85 1.22 0.98 0.95 1.2 1.01 50 M050I 0.33 1.61 0.91 1.09 0.9 0.55 50 M050K 0.49 0.80 0.67 0.79 1.1 1.07 50 M050L 0.91 0.76 1.02 0.96 1.1 1.00 50 M050N 0.35 1.03 0.86 1.07 1.0 1.11 50 M050Q 0.76 1.23 0.93 1.03 1.1 1.01 50 M050R 0.25 1.38 0.73 1.07 1.0 0.82 50 M050S 0.81 1.08 0.89 1.05 1.0 1.08 50 M050T 0.87 1.05 0.90 1.04 1.1 1.38 50 M050V 0.70 1.08 0.82 1.02 1.1 0.82 50 M050W 1.06 1.10 0.80 0.78 1.0 1.16 50 M050Y 0.70 1.03 0.87 0.89 1.0 1.19 51 V051A 0.38 1.41 1.25 1.22 0.9 0.43 51 V051C 0.91 1.02 1.16 1.02 1.1 0.41 51 V051D 0.34 1.02 1.32 1.12 1.0 0.50 51 V051E 0.39 1.17 1.59 1.26 1.0 0.59 51 V051H 0.86 0.59 1.06 0.98 1.2 0.79 51 V051I 0.69 0.79 1.23 1.12 1.1 0.95 51 V051L 0.48 0.73 1.21 0.87 1.0 0.59 51 V051M 0.60 0.97 1.07 1.10 1.0 0.67 51 V051Q 0.28 1.26 1.81 1.14 0.9 0.40 51 V051S 0.32 1.84 1.95 1.43 0.9 0.35 51 V051T 0.46 0.98 1.16 1.03 0.9 0.75 51 V051Y 0.25 1.20 1.58 1.76 0.9 0.31 52 P052A 0.56 1.22 1.25 1.17 0.7 0.59 52 P052C 0.34 1.36 1.56 0.94 1.0 0.44 52 P052D 0.79 1.27 1.50 1.21 0.9 0.76 52 P052E 0.89 1.12 1.54 1.20 0.9 0.75 52 P052F 0.41 0.87 1.13 1.14 0.9 0.51 52 P052G 0.44 1.05 1.42 1.24 0.8 0.53 52 P052H 0.45 0.97 1.28 1.04 0.9 0.47 52 P052I 0.45 1.33 1.50 1.11 0.8 0.61 52 P052K 0.38 0.86 1.09 1.35 0.8 0.53 52 P052L 0.46 1.33 1.24 1.32 0.8 0.61 52 P052M 0.43 1.40 1.30 1.06 0.7 0.54 52 P052Q 0.43 0.83 1.48 1.20 0.8 0.63 52 P052R 0.33 1.02 1.31 1.26 0.7 0.58 52 P052S 0.51 1.02 1.55 1.26 0.8 0.60 52 P052T 0.47 1.23 1.73 1.09 0.8 0.61 52 P052V 0.31 1.79 1.63 1.03 1.0 0.50 52 P052W 0.36 1.49 1.34 1.43 1.0 0.77 52 P052Y 0.35 1.55 1.42 1.32 1.0 0.55 53 S053A 1.37 1.07 1.15 1.03 1.0 0.87 53 S053E 1.52 1.05 1.16 1.12 1.0 0.98 53 S053F 1.19 0.91 1.05 0.87 1.0 1.11 53 S053G 1.72 1.15 1.19 0.94 1.0 0.86 53 S053H 1.35 0.96 1.02 0.96 1.1 0.84 53 S053I 1.22 0.97 1.10 0.80 1.0 0.90 53 S053K 1.36 0.89 0.93 0.76 1.1 0.95 53 S053L 1.18 0.92 0.97 1.00 1.1 0.90 53 S053M 1.54 1.01 0.98 0.97 0.8 0.80 53 S053N 1.48 0.95 1.04 1.15 1.1 0.87 53 S053P 0.46 1.01 1.39 0.94 0.9 0.85 53 S053Q 0.76 0.85 1.30 1.09 1.1 1.05 53 S053R 1.06 0.68 0.82 0.87 1.1 1.00 53 S053T 1.33 1.05 1.23 0.85 1.0 0.94 53 S053V 1.13 1.11 1.20 1.10 1.1 0.95 53 S053W 1.49 0.86 1.02 0.80 0.9 0.98 54 E054A 0.89 0.97 1.07 0.83 0.6 0.66 54 E054C 0.71 0.94 1.05 0.85 0.8 0.68 54 E054F 0.51 0.86 0.97 0.93 0.7 0.63 54 E054G 0.38 1.27 0.59 1.04 0.5 0.42 54 E054H 0.73 0.69 0.80 0.96 0.8 0.67 54 E054K 0.35 1.03 1.14 1.07 0.8 0.60 54 E054L 0.49 1.00 1.02 0.87 0.8 0.71 54 E054M 0.63 1.06 0.99 1.03 0.7 0.61 54 E054N 0.97 0.99 1.03 1.06 0.8 0.76 54 E054P 0.19 0.47 1.13 1.34 0.6 0.17 54 E054Q 0.97 1.00 0.99 1.04 0.8 0.90 54 E054R 0.24 1.47 1.83 1.68 0.6 0.55 54 E054S 0.98 0.97 0.97 0.96 0.8 0.69 54 E054T 0.52 1.02 1.11 0.93 0.6 0.70 54 E054V 0.41 1.12 1.34 1.11 0.6 0.78 54 E054W 0.31 1.18 1.18 1.01 0.6 0.71 54 E054Y 0.42 1.03 0.99 1.00 0.8 0.69 55 T055A 1.11 0.63 0.98 1.00 1.0 0.96 55 T055C 1.41 0.64 1.06 0.89 1.1 0.86 55 T055D 0.76 1.01 1.26 0.94 1.1 1.06 55 T055F 0.67 0.62 0.78 0.84 0.9 0.92 55 T055G 1.21 1.00 0.90 0.97 1.1 0.85 55 T055H 1.06 1.14 0.98 0.96 1.1 1.04 55 T055I 0.96 1.08 0.97 0.89 1.0 1.02 55 T055K 1.27 0.59 0.87 0.98 1.0 1.09 55 T055L 1.39 0.80 1.30 0.96 1.1 0.95 55 T055M 0.92 0.85 1.19 0.99 1.0 1.09 55 T055P 0.94 0.90 1.20 0.86 1.0 1.23 55 T055Q 1.06 0.87 1.20 0.91 1.1 1.06 55 T055R 1.14 0.54 0.81 0.90 1.0 1.01 55 T055S 1.00 1.03 1.32 0.94 1.1 0.99 55 T055V 0.98 0.54 1.20 0.97 1.0 1.10 55 T055W 1.06 0.68 0.81 0.92 1.0 0.95 55 T055Y 0.97 0.90 0.97 0.91 1.0 0.91 56 N056A 0.31 1.18 1.27 1.14 0.4 0.34 56 N056D 1.09 0.79 0.89 0.84 1.2 0.99 56 N056E 0.67 0.91 0.98 0.91 0.7 0.69 56 N056F 0.27 1.02 1.00 1.31 0.6 0.31 56 N056G 0.29 1.61 1.06 1.22 0.4 0.46 56 N056H 0.39 1.08 1.07 0.95 0.8 0.81 56 N056I 0.24 1.69 1.26 1.41 0.6 0.47 56 N056K 0.21 2.07 1.45 1.86 0.5 0.38 56 N056L 0.23 1.26 1.81 1.66 0.7 0.34 56 N056M 0.26 1.50 1.24 1.23 0.5 0.36 56 N056P 0.26 0.95 1.32 0.94 0.8 0.62 56 N056Q 0.29 1.74 1.29 1.22 0.8 0.41 56 N056R 0.17 4.90 3.96 2.20 0.5 0.27 56 N056S 0.99 0.78 0.97 0.92 0.9 0.77 56 N056T 0.58 0.90 1.08 1.04 0.6 0.65 56 N056V 0.27 1.36 1.29 0.99 0.5 0.49 56 N056W 0.36 1.28 1.33 1.16 0.6 0.48 56 N056Y 0.25 1.30 1.25 1.30 0.7 0.41 57 P057A 0.61 0.95 1.08 1.03 0.5 0.66 57 P057C 0.50 1.04 1.18 0.95 0.8 0.65 57 P057D 0.52 1.11 1.42 1.14 0.9 0.87 57 P057E 0.38 1.23 1.53 1.23 0.8 0.87 57 P057F 0.59 0.93 0.98 0.92 0.3 0.75 57 P057G 0.42 1.29 1.19 1.12 0.3 0.69 57 P057I 0.25 2.20 2.00 1.60 0.4 0.29 57 P057K 0.24 1.51 1.84 1.09 0.3 0.34 57 P057L 0.24 2.59 2.00 1.46 0.4 0.28 57 P057M 0.36 1.08 1.11 0.97 0.4 0.40 57 P057N 0.35 1.17 1.67 1.11 0.7 0.73 57 P057Q 0.35 1.25 1.38 1.04 0.5 0.65 57 P057R 0.23 2.31 3.14 1.52 0.4 0.42 57 P057S 0.39 0.91 1.10 0.97 0.5 0.65 57 P057T 0.25 2.53 1.97 2.27 0.5 0.56 57 P057V 0.22 3.61 5.95 3.50 0.3 0.48 57 P057W 1.03 0.61 1.05 0.94 0.7 0.86 58 F058A 0.55 1.18 1.32 1.15 0.6 0.61 58 F058C 0.95 1.08 1.21 0.93 1.1 0.92 58 F058D 0.52 1.18 1.32 0.97 1.0 0.93 58 F058E 0.87 0.87 1.20 1.09 0.9 1.05 58 F058G 0.91 1.21 1.26 1.00 1.1 0.76 58 F058H 0.98 0.96 1.34 0.89 0.9 0.99 58 F058I 0.64 0.88 1.07 0.94 0.8 1.00 58 F058K 0.44 1.15 1.36 1.09 0.6 0.63 58 F058L 0.89 0.99 1.16 0.89 0.9 0.86 58 F058M 1.01 1.08 1.24 0.91 0.8 0.82 58 F058N 0.86 1.18 1.25 0.87 0.9 0.91 58 F058P 0.23 0.71 1.00 0.89 0.6 0.22 58 F058Q 0.60 1.22 1.20 0.93 0.6 0.80 58 F058R 0.49 0.75 1.06 0.95 1.0 0.73 58 F058S 0.61 1.21 1.10 1.03 0.6 0.81 58 F058T 0.36 1.36 1.76 1.16 0.7 1.01 58 F058V 0.73 1.01 1.09 1.05 0.7 0.98 58 F058Y 1.16 1.19 0.90 1.00 0.9 1.09 59 Q059A 1.27 0.91 1.18 0.96 0.9 0.96 59 Q059C 0.89 1.08 1.26 1.06 1.2 0.92 59 Q059D 1.42 1.09 1.31 0.88 1.2 1.01 59 Q059E 1.42 1.11 1.15 0.85 1.3 0.94 59 Q059F 1.18 0.97 1.13 0.85 0.9 0.93 59 Q059G 0.92 1.06 1.05 1.00 0.7 0.75 59 Q059H 1.24 0.91 1.00 1.14 1.0 0.91 59 Q059K 1.31 0.83 0.87 0.87 0.9 0.94 59 Q059L 1.21 1.10 1.12 1.04 1.1 1.01 59 Q059M 1.26 1.18 1.08 0.95 1.1 0.95 59 Q059N 1.15 1.12 1.16 1.01 1.0 0.98 59 Q059P 0.27 1.86 2.01 1.47 0.8 0.43 59 Q059R 0.82 0.78 0.71 0.81 1.0 0.95 59 Q059S 1.25 1.13 1.15 0.94 0.8 0.97 59 Q059T 1.37 1.10 1.04 1.02 0.9 0.90 59 Q059V 1.38 1.14 1.14 1.14 1.0 1.21 59 Q059W 0.24 1.36 1.62 1.16 1.0 0.46 59 Q059Y 1.12 1.08 1.21 1.08 0.9 0.86 60 D060A 0.43 1.01 1.21 0.99 0.2 0.68 60 D060C 0.49 0.81 0.94 0.89 0.5 0.56 60 D060E 0.32 0.89 1.23 0.94 0.5 0.45 60 D060F 0.25 0.35 1.00 0.71 0.1 0.34 60 D060G 1.09 0.80 0.93 0.89 0.4 0.91 60 D060H 0.31 0.66 1.29 0.95 0.2 0.50 60 D060I 0.33 0.50 1.15 0.83 0.1 0.61 60 D060L 0.27 0.54 1.07 0.88 0.1 0.41 60 D060M 0.27 0.87 1.26 1.16 0.2 0.43 60 D060N 0.32 0.77 1.19 1.11 0.2 0.55 60 D060P 0.85 0.64 0.83 0.73 0.1 0.59 60 D060Q 0.26 0.97 1.35 1.03 0.2 0.57 60 D060R 0.35 0.31 0.65 0.63 0.1 0.62 60 D060S 0.40 0.83 0.96 1.00 0.2 0.74 60 D060T 0.30 0.95 1.72 1.28 0.2 0.78 60 D060V 0.39 0.77 0.91 0.98 0.1 0.74 60 D060W 0.21 0.57 1.17 1.22 0.1 0.35 60 D060Y 0.28 0.58 0.93 0.73 0.2 0.47 61 N061A 1.66 1.22 1.11 1.09 1.0 0.95 61 N061C 1.41 0.95 0.96 0.90 1.1 1.11 61 N061D 1.25 1.19 1.21 0.85 1.2 1.14 61 N061E 1.53 1.21 1.08 1.08 1.2 1.08 61 N061F 1.50 1.00 0.90 0.80 1.0 0.89 61 N061G 1.45 1.01 1.06 1.01 1.0 0.80 61 N061H 1.46 1.15 1.00 0.93 1.2 0.89 61 N061I 1.32 1.25 1.00 0.71 1.2 1.10 61 N061K 1.20 0.89 1.00 0.76 0.9 1.11 61 N061L 1.34 0.96 1.00 0.88 1.1 1.07 61 N061M 1.28 0.98 1.01 1.04 1.0 1.06 61 N061P 1.42 1.47 1.04 0.78 1.0 1.40 61 N061Q 1.27 0.90 1.08 0.88 1.0 1.14 61 N061R 1.42 0.67 0.71 0.86 0.8 1.09 61 N061S 1.06 1.00 0.98 0.88 0.9 1.51 61 N061T 1.14 0.98 0.98 0.99 1.1 1.19 61 N061V 1.43 1.02 1.03 0.77 1.0 1.19 61 N061W 1.42 1.12 0.80 0.83 1.1 0.94 61 N061Y 1.31 1.04 0.97 0.98 1.2 0.90 62 N062A 1.20 0.77 0.76 0.88 1.1 1.18 62 N062C 1.57 1.18 1.16 0.82 0.3 0.63 62 N062D 1.48 1.40 1.18 0.91 1.1 0.67 62 N062E 1.42 1.19 1.19 0.92 1.1 0.59 62 N062F 2.06 0.75 1.07 0.87 1.1 0.37 62 N062G 1.41 1.03 0.83 0.84 1.3 0.78 62 N062I 0.95 0.81 0.87 0.69 1.3 0.74 62 N062K 1.23 1.05 0.97 1.02 0.9 0.48 62 N062L 1.79 0.87 0.80 1.07 1.4 0.63 62 N062M 1.76 1.30 1.12 1.07 1.1 0.58 62 N062Q 1.45 1.32 1.23 1.06 1.2 0.60 62 N062R 1.33 1.13 0.73 0.94 0.9 0.29 62 N062S 0.65 1.14 0.97 0.91 1.0 1.06 62 N062T 0.96 1.21 0.97 0.86 1.1 1.01 62 N062V 1.43 0.86 1.00 0.57 1.1 0.56 62 N062W 1.56 1.27 1.25 0.79 1.1 0.11 62 N062Y 1.70 0.92 0.79 1.09 1.2 0.37 63 S063A 1.12 0.94 1.12 0.98 1.1 0.88 63 S063C 1.56 1.31 0.97 0.69 1.3 0.77 63 S063D 1.42 0.90 0.86 0.84 1.4 0.81 63 S063E 1.50 1.13 1.03 0.93 1.3 1.00 63 S063F 1.26 0.91 0.73 0.88 1.0 0.77 63 S063G 1.46 0.67 0.79 0.83 0.9 1.21 63 S063H 1.41 0.92 0.95 0.80 1.0 0.90 63 S063K 1.62 1.03 0.75 0.89 0.3 0.82 63 S063L 1.46 1.22 0.86 1.02 1.0 0.92 63 S063M 1.48 1.02 0.86 1.17 0.9 1.04 63 S063N 1.42 0.97 1.00 0.97 1.2 0.85 63 S063P 0.84 0.62 0.71 0.71 0.6 0.67 63 S063Q 1.55 1.36 0.81 1.05 1.0 0.98 63 S063R 1.58 0.93 0.65 0.83 0.1 1.03 63 S063T 1.03 1.33 1.03 1.01 1.0 0.93 63 S063V 1.19 1.13 0.88 0.98 0.7 1.35 63 S063W 1.26 0.84 0.93 0.67 0.9 2.18 63 S063Y 1.38 1.02 0.72 0.93 0.8 0.90 65 G065Q 0.23 1.74 2.07 2.34 1.2 0.66 66 T066S 1.10 0.87 0.95 0.89 0.6 0.81 67 H067A 1.37 0.43 0.24 0.50 0.5 0.34 67 H067C 1.36 0.46 0.24 0.52 0.3 0.29 67 H067F 1.13 0.64 0.50 0.81 0.1 0.33 67 H067I 1.55 0.51 0.20 0.47 0.2 0.42 67 H067L 1.31 0.37 0.14 0.47 0.3 0.16 67 H067M 1.34 0.56 0.31 0.66 0.6 0.42 67 H067N 1.12 0.76 0.31 0.65 0.1 0.62 67 H067P 1.01 0.43 0.18 0.50 0.8 0.51 67 H067S 1.26 0.55 0.28 0.55 0.1 0.39 67 H067T 1.23 0.57 0.36 0.69 0.1 0.52 68 V068A 1.00 1.79 1.11 1.30 1.0 0.06 68 V068C 1.05 1.11 1.10 1.07 0.8 0.70 68 V068I 1.19 1.15 0.96 0.82 1.2 0.32 68 V068T 0.94 1.17 1.06 0.79 0.6 0.42 69 A069C 0.36 1.66 0.92 1.19 0.7 0.45 69 A069G 0.88 0.73 0.95 1.04 0.9 1.02 69 A069H 0.17 39.03 2.24 0.72 0.7 0.08 69 A069M 0.19 7.17 0.69 0.55 0.5 0.06 69 A069S 0.85 0.61 0.70 1.17 0.9 0.93 69 A069T 0.48 1.58 0.96 1.02 1.0 0.72 71 T071A 0.44 1.17 1.02 1.07 0.1 0.59 71 T071D 0.21 41.12 34.56 1.45 0.2 0.06 71 T071E 0.25 2.16 1.92 1.03 0.1 0.33 71 T071I 0.80 0.74 1.19 1.08 0.5 1.07 71 T071K 0.21 37.02 45.54 2.17 0.1 0.17 71 T071S 1.14 0.87 1.17 1.17 0.5 0.89 71 T071V 0.74 0.85 1.00 0.99 0.5 0.86 72 V072A 0.84 0.95 1.00 0.94 0.8 0.89 72 V072C 0.71 1.13 1.02 1.10 0.8 0.88 72 V072D 0.19 2.54 1.66 1.93 0.7 0.19 72 V072E 0.50 1.14 1.08 1.13 0.8 0.62 72 V072F 0.71 0.96 1.06 0.96 0.7 0.74 72 V072G 0.35 1.52 1.06 1.36 0.8 0.65 72 V072H 0.35 1.05 1.01 1.17 0.8 0.57 72 V072I 1.16 1.12 1.03 0.97 1.0 0.79 72 V072K 0.19 2.81 2.06 2.76 1.7 0.30 72 V072L 1.00 1.16 1.07 0.97 0.9 0.67 72 V072Q 0.27 1.63 1.54 1.67 0.6 0.64 72 V072S 0.36 1.36 1.41 1.34 0.8 0.91 72 V072T 0.63 1.37 1.01 1.09 0.9 0.99 73 A073C 0.85 1.03 1.08 1.03 0.9 0.93 73 A073E 0.47 1.62 1.22 1.13 0.2 0.78 73 A073G 0.96 0.85 1.01 1.14 0.8 1.00 73 A073I 0.17 22.54 15.70 6.07 0.1 0.30 73 A073K 0.18 3.45 2.48 2.56 0.1 0.27 73 A073M 0.24 1.71 1.42 1.48 0.3 0.43 73 A073Q 0.55 1.31 1.33 1.14 0.5 0.93 73 A073S 1.02 1.35 0.94 1.00 0.8 1.06 73 A073T 0.71 1.27 1.06 1.15 0.6 1.11 73 A073V 0.38 1.42 1.19 1.46 0.1 0.83 74 A074G 1.04 0.89 0.85 1.06 0.2 1.00 77 N077C 0.23 0.95 0.12 0.36 0.2 0.14 77 N077E 0.20 1.17 0.13 0.35 0.2 0.07 77 N077I 0.23 0.63 0.09 0.28 0.2 0.08 77 N077K 0.18 1.28 0.06 0.36 0.2 0.12 77 N077L 0.19 2.18 0.24 0.77 0.1 0.12 77 N077M 0.21 0.94 0.11 0.32 0.3 0.06 77 N077R 0.18 2.49 0.10 0.93 0.1 0.16 78 S078A 1.21 1.08 1.10 1.03 1.1 0.91 78 S078C 1.23 1.03 0.77 0.88 1.5 0.83 78 S078D 1.33 1.10 0.83 0.88 1.7 0.90 78 S078E 1.04 1.05 0.87 0.96 1.1 0.91 78 S078F 1.11 0.95 0.64 0.98 0.5 0.97 78 S078G 1.28 1.14 0.83 0.92 0.6 0.88 78 S078I 1.00 1.03 0.70 0.96 0.3 0.99 78 S078K 1.25 0.98 0.62 0.94 0.3 0.92 78 S078L 0.68 1.01 0.78 0.92 0.8 0.96 78 S078M 1.03 1.06 1.09 0.99 1.2 1.04 78 S078N 1.19 1.04 0.87 1.16 1.6 1.00 78 S078Q 1.12 1.11 0.94 1.09 1.4 1.36 78 S078R 1.22 1.02 0.52 0.81 0.7 1.15 78 S078T 1.07 1.17 1.02 0.99 1.4 1.09 78 S078V 1.13 1.16 0.97 0.91 0.5 0.90 78 S078W 1.00 1.31 0.67 1.02 0.3 1.08 78 S078Y 1.06 0.97 0.68 1.12 0.6 1.06 79 I079C 1.22 0.73 1.12 1.02 0.2 0.91 79 I079E 1.28 0.71 1.02 0.98 0.1 1.00 79 I079F 1.23 0.93 1.22 1.03 0.9 0.95 79 I079V 1.10 0.68 1.15 1.02 0.1 0.97 79 I079W 1.13 0.81 1.15 1.18 0.1 1.00 79 I079Y 1.19 0.76 1.26 0.92 1.0 1.25 80 G080C 0.19 0.60 1.75 1.16 0.1 0.36 81 V081D 0.24 1.35 0.77 0.60 0.1 0.14 81 V081I 1.15 1.09 0.82 1.05 0.3 0.88 81 V081T 0.94 1.17 0.79 1.00 0.2 0.67 81 V081Y 0.88 1.22 0.77 1.08 0.1 0.84 82 L082G 0.21 2.20 1.71 1.50 0.1 0.36 82 L082V 0.78 1.21 1.19 1.10 0.2 1.13 82 L082W 0.17 10.29 8.50 4.18 0.7 0.37 84 V084A 1.27 0.84 0.96 0.82 0.7 1.08 84 V084C 1.15 0.77 0.75 0.79 0.8 0.97 84 V084G 0.29 0.75 0.84 0.86 0.5 0.66 84 V084I 1.08 0.96 0.99 0.68 0.5 0.99 84 V084L 0.51 0.66 0.91 1.00 0.3 1.07 84 V084M 0.89 0.91 0.68 0.87 0.3 1.20 84 V084N 0.67 0.75 0.98 0.88 0.8 1.09 84 V084S 0.81 0.79 0.64 0.85 0.5 1.00 84 V084T 1.06 0.95 0.42 0.70 0.7 0.92 85 A085C 0.64 0.84 0.85 0.99 0.8 0.73 85 A085G 0.77 0.93 0.92 0.97 0.9 0.94 85 A085S 0.90 0.94 0.94 0.97 0.9 0.93 85 A085T 0.43 1.35 1.11 0.88 0.6 0.95 85 A085V 0.20 2.50 2.45 2.31 0.7 0.49 86 P086A 0.45 1.30 1.13 1.29 0.7 1.08 86 P086D 0.52 1.20 0.80 1.21 0.5 0.95 86 P086E 0.46 0.88 1.20 1.02 0.4 1.10 86 P086G 0.37 1.41 0.91 1.28 0.1 0.76 86 P086M 0.27 1.95 1.84 1.83 0.1 1.02 86 P086N 0.54 1.25 1.13 1.14 0.7 1.07 86 P086Q 0.25 1.54 1.60 1.99 0.1 0.88 86 P086R 0.19 3.54 3.82 2.73 0.7 0.72 86 P086S 0.53 1.15 1.15 1.06 0.7 1.21 86 P086T 0.28 1.73 1.80 1.87 0.2 1.05 86 P086W 0.42 1.35 1.52 1.25 0.4 1.41 86 P086Y 0.39 1.46 1.19 1.70 0.9 1.38 87 S087A 1.11 1.20 1.08 1.01 0.9 0.82 87 S087C 1.16 1.11 0.98 0.86 1.1 0.86 87 S087D 1.12 1.29 1.05 0.95 1.5 0.89 87 S087E 1.19 1.03 1.04 1.00 1.4 0.96 87 S087F 0.92 1.36 0.88 1.06 0.5 0.95 87 S087G 1.16 1.16 0.91 1.03 0.8 0.85 87 S087I 0.56 1.40 0.81 1.01 0.4 0.90 87 S087K 1.39 0.87 0.72 1.10 0.4 0.85 87 S087L 1.07 1.31 0.95 1.07 0.8 0.98 87 S087M 1.02 1.34 0.99 1.08 0.7 1.04 87 S087N 1.32 1.23 1.04 0.96 1.0 0.86 87 S087Q 0.81 1.34 0.93 0.96 0.8 0.87 87 S087R 1.23 1.06 0.73 0.99 0.2 0.82 87 S087T 1.08 1.17 1.00 1.10 0.9 1.16 87 S087V 0.92 1.33 0.95 1.17 0.9 1.15 87 S087W 0.91 1.44 1.01 1.26 0.5 1.06 88 A088C 0.78 1.12 1.30 1.05 0.9 1.02 88 A088D 0.27 1.44 1.63 1.25 0.7 0.68 88 A088E 0.17 11.44 17.45 1.68 0.6 0.16 88 A088G 0.65 1.19 1.28 1.06 0.9 1.07 88 A088K 0.21 2.38 2.98 1.68 0.8 0.67 88 A088L 0.62 1.20 1.17 0.93 0.8 1.06 88 A088M 0.45 1.03 1.50 0.98 0.4 0.73 88 A088N 0.67 0.97 1.11 1.08 0.6 1.17 88 A088P 0.21 2.19 3.40 2.03 0.9 0.62 88 A088Q 0.22 1.86 1.99 1.23 0.5 0.52 88 A088S 0.84 0.94 1.31 0.91 0.9 1.09 88 A088T 0.86 1.28 1.29 0.94 1.0 1.08 88 A088V 0.87 1.22 1.41 0.94 0.9 1.11 89 S089C 0.91 1.14 1.14 0.99 0.9 0.92 89 S089D 1.20 1.35 1.04 1.09 0.8 0.96 89 S089E 0.92 1.07 1.17 0.95 0.8 0.93 89 S089F 0.65 1.14 1.27 0.90 0.8 1.16 89 S089G 0.88 1.13 1.10 1.13 0.8 1.04 89 S089H 0.99 0.86 1.23 1.09 0.6 1.09 89 S089K 0.98 0.99 1.06 1.01 0.8 0.88 89 S089L 0.41 1.08 1.52 1.40 1.3 0.93 89 S089M 0.43 1.28 1.34 1.17 1.4 0.86 89 S089R 0.71 0.67 1.08 1.06 0.8 0.94 89 S089V 0.66 1.31 1.27 1.17 0.7 1.34 89 S089W 0.37 1.19 1.84 1.30 1.2 1.05 89 S089Y 0.75 1.22 1.34 1.00 0.7 1.13 90 L090A 0.35 1.29 1.22 1.35 0.7 0.85 90 L090D 0.20 2.40 2.05 2.19 0.6 0.47 90 L090E 0.23 1.61 1.38 1.49 1.0 0.52 90 L090F 0.30 1.57 0.81 1.39 0.3 0.34 90 L090G 0.28 0.21 0.15 0.22 0.9 0.11 90 L090H 0.23 2.00 2.18 2.26 1.0 0.88 90 L090M 0.78 1.07 1.04 0.94 1.0 0.95 90 L090P 0.27 1.56 1.73 1.61 0.9 0.88 90 L090Q 0.44 1.22 1.21 1.20 1.1 1.05 90 L090S 0.24 1.57 1.85 1.57 0.7 0.93 90 L090T 0.21 3.87 3.31 2.49 0.8 0.96 90 L090V 0.77 1.20 1.08 1.18 0.8 1.12 91 Y091A 0.25 0.60 1.29 1.22 0.9 0.67 91 Y091C 0.23 0.99 2.01 1.14 1.1 0.54 91 Y091D 0.31 0.90 1.51 1.27 1.1 0.80 91 Y091F 1.07 0.60 1.21 1.23 1.1 1.00 91 Y091H 0.80 0.71 1.16 1.04 1.0 0.99 91 Y091I 0.22 1.01 2.17 1.25 1.2 0.58 91 Y091L 0.18 1.59 2.82 1.67 1.0 0.49 91 Y091M 0.27 1.09 1.56 1.13 1.1 0.62 91 Y091Q 0.16 7.64 26.89 1.98 1.2 0.25 91 Y091S 0.25 0.90 1.68 1.44 0.8 0.86 91 Y091T 0.17 3.68 8.06 2.67 0.9 0.61 91 Y091V 0.23 0.89 1.92 1.46 1.0 0.70 92 A092C 0.29 2.61 2.00 1.71 0.6 0.33 92 A092G 0.55 1.16 1.46 1.30 0.8 0.67 92 A092I 0.33 1.73 1.53 1.55 0.7 0.31 92 A092M 0.21 2.49 2.62 2.92 0.6 0.16 92 A092N 0.18 6.44 7.31 5.48 0.7 0.15 92 A092P 0.26 1.62 2.34 2.13 0.9 0.47 92 A092S 1.04 0.85 0.94 1.22 1.1 0.87 92 A092T 0.73 1.10 1.14 0.98 0.9 0.96 92 A092V 0.30 1.40 1.31 1.73 0.6 0.50 93 V093A 0.31 1.09 1.32 1.22 0.9 0.68 93 V093C 0.61 1.02 1.24 1.00 0.9 0.86 93 V093D 0.21 2.38 3.40 2.01 1.1 0.67 93 V093F 0.22 1.32 2.23 1.46 1.0 0.61 93 V093G 0.23 0.60 1.00 0.61 1.1 0.18 93 V093L 0.58 1.39 1.12 1.01 0.8 0.98 93 V093S 0.29 0.17 0.35 0.27 0.9 0.12 93 V093T 0.33 1.46 1.70 1.37 1.1 1.04 94 K094C 0.22 1.33 1.37 1.05 1.0 0.17 94 K094E 0.21 0.66 0.92 0.67 0.8 0.06 94 K094L 0.30 0.26 0.32 0.28 1.1 0.06 94 K094N 0.28 0.69 3.31 0.56 0.8 0.08 94 K094Q 0.42 1.19 1.22 0.90 1.0 0.72 94 K094R 0.41 1.36 1.48 1.32 0.8 0.39 94 K094S 0.19 4.15 3.79 2.53 1.0 0.24 94 K094V 0.21 0.75 1.10 0.67 0.8 0.12 95 V095A 0.44 0.85 0.53 0.71 1.0 0.87 95 V095C 1.03 0.96 0.64 0.87 1.0 1.11 95 V095G 0.43 0.97 0.34 0.83 1.0 0.86 95 V095S 0.91 1.07 0.82 0.96 1.1 1.11 95 V095T 0.90 1.23 0.95 1.04 1.1 0.98 96 L096F 0.45 2.00 0.80 1.35 0.9 0.55 96 L096I 0.76 1.64 0.85 1.02 1.2 0.35 96 L096M 0.91 1.53 1.09 1.23 0.9 0.46 96 L096V 0.95 1.42 0.85 1.31 1.1 0.08 96 L096W 0.20 5.01 1.57 2.17 1.0 0.33 97 G097A 0.91 1.55 0.95 1.33 1.0 0.77 97 G097C 1.01 1.66 1.07 1.08 1.0 0.49 97 G097D 1.55 1.43 0.79 1.20 1.0 0.76 97 G097E 1.14 1.38 0.78 1.06 1.1 0.71 97 G097F 0.29 1.93 1.01 1.36 0.9 0.29 97 G097H 0.85 1.26 1.10 1.01 1.0 0.47 97 G097K 1.23 1.17 0.63 1.00 1.1 0.77 97 G097L 0.77 1.43 1.11 1.24 1.1 0.70 97 G097M 0.84 1.32 1.04 1.18 1.1 0.91 97 G097P 0.39 2.35 1.56 1.34 1.1 0.69 97 G097Q 0.97 1.36 0.77 1.03 1.2 0.98 97 G097R 1.22 0.97 0.64 1.02 1.0 0.92 97 G097S 0.98 1.45 1.12 1.07 0.9 0.95 97 G097T 1.02 1.23 0.93 1.10 1.0 1.09 97 G097V 0.54 1.56 1.09 1.22 1.0 0.95 97 G097W 0.23 2.95 1.54 1.49 1.0 0.34 97 G097Y 0.37 1.37 0.93 1.04 0.9 0.34 98 A098C 1.10 0.86 1.07 1.06 1.2 0.94 98 A098D 1.18 0.87 1.36 1.19 1.2 0.91 98 A098E 1.08 0.49 1.20 1.06 0.9 1.24 98 A098F 0.73 0.54 1.00 1.02 1.0 1.16 98 A098G 1.20 0.94 1.27 1.09 0.9 0.93 98 A098H 1.26 0.70 1.08 0.97 1.0 0.99 98 A098I 0.98 0.93 1.00 1.08 0.9 1.39 98 A098L 0.96 0.63 1.09 1.01 1.0 1.05 98 A098P 1.13 0.87 1.19 1.09 1.0 0.79 98 A098Q 0.89 0.76 1.13 1.05 1.0 1.09 98 A098R 1.22 0.70 1.00 1.11 1.0 0.95 98 A098S 1.20 0.85 1.12 1.12 0.8 1.01 98 A098T 0.98 0.74 1.09 0.99 1.0 1.36 98 A098V 0.99 0.91 1.17 0.97 0.9 1.70 98 A098Y 0.89 0.75 1.20 1.01 0.8 1.37 99 D099A 0.81 1.07 0.65 1.04 0.8 0.62 99 D099C 0.71 1.49 0.78 1.08 1.1 0.62 99 D099E 1.04 1.37 0.80 1.03 1.0 0.80 99 D099F 0.50 1.14 0.53 1.08 1.0 0.44 99 D099H 0.79 1.17 0.53 0.98 0.9 0.65 99 D099I 0.44 1.59 0.64 1.10 1.0 0.55 99 D099K 0.94 0.72 0.43 1.00 1.0 0.75 99 D099L 0.34 1.20 0.47 0.93 1.1 0.57 99 D099M 0.59 1.38 0.65 1.18 0.9 0.66 99 D099N 1.06 1.09 0.74 0.99 1.1 0.88 99 D099P 0.39 1.98 0.89 1.21 1.0 0.40 99 D099Q 0.98 1.08 0.77 1.15 1.0 0.65 99 D099R 0.87 0.54 0.42 0.86 1.1 0.83 99 D099S 0.87 1.00 0.60 0.97 0.9 0.94 99 D099T 0.70 1.08 0.70 1.10 0.9 0.97 99 D099V 0.43 1.71 0.75 1.08 0.9 0.61 99 D099W 0.58 1.22 0.57 0.89 0.8 0.88 99 D099Y 0.50 1.43 0.60 1.07 0.9 0.60 100 G100A 0.94 0.95 1.13 0.96 1.0 0.35 100 G100D 0.77 1.41 1.35 1.08 0.9 0.34 100 G100E 0.54 1.66 1.46 1.25 1.0 0.30 100 G100F 0.53 1.04 1.32 1.22 0.9 0.10 100 G100H 0.55 1.41 1.18 1.05 0.9 0.28 100 G100K 0.65 1.46 1.00 1.22 0.9 0.31 100 G100M 1.13 1.42 1.16 1.20 0.8 0.17 100 G100N 1.09 1.25 1.29 1.31 1.0 0.41 100 G100Q 0.66 1.57 1.18 1.38 1.0 0.35 100 G100R 0.68 1.09 0.89 1.03 0.9 0.29 100 G100S 0.79 1.28 1.35 1.15 0.9 0.35 100 G100T 0.34 2.17 1.64 1.46 1.0 0.18 100 G100V 0.31 1.98 1.55 1.39 1.0 0.07 100 G100Y 0.49 1.58 1.27 1.05 1.0 0.20 101 S101A 1.27 1.38 1.00 1.09 1.1 1.08 101 S101C 1.24 1.14 0.67 0.90 1.2 0.61 101 S101E 1.35 1.52 1.19 1.14 1.1 0.71 101 S101F 0.96 1.02 0.73 0.97 1.0 1.13 101 S101G 0.38 1.30 0.46 0.67 1.1 0.21 101 S101I 1.01 1.22 0.75 0.86 1.2 0.91 101 S101K 1.28 1.15 0.62 1.00 1.1 0.99 101 S101L 1.10 1.21 0.80 1.00 1.0 1.21 101 S101M 1.01 1.22 0.79 1.08 1.1 1.21 101 S101N 1.24 1.46 0.99 1.10 1.1 1.03 101 S101P 0.25 3.64 1.39 1.83 1.1 0.30 101 S101Q 0.59 1.56 0.79 1.05 1.0 1.24 101 S101R 1.20 1.04 0.65 0.90 1.0 0.94 101 S101T 0.94 1.34 0.68 1.16 1.0 1.12 101 S101V 0.92 1.39 0.74 1.18 0.9 1.19 101 S101Y 0.72 1.04 0.48 0.92 1.0 1.54 102 G102A 1.12 1.46 1.31 1.19 1.0 0.31 102 G102S 0.77 1.61 1.10 1.04 1.1 0.11 103 Q103A 1.09 0.93 0.93 0.89 1.0 0.92 103 Q103C 1.19 1.10 1.05 0.97 1.0 0.63 103 Q103E 1.21 1.38 1.15 1.05 1.0 0.64 103 Q103F 1.02 0.82 0.57 0.83 0.9 0.91 103 Q103G 0.39 1.48 1.06 1.34 1.1 0.43 103 Q103H 0.89 1.35 0.89 0.93 0.9 0.65 103 Q103I 1.06 0.88 0.89 0.87 1.1 0.82 103 Q103K 0.17 2.63 1.36 1.25 1.0 0.45 103 Q103L 0.44 0.87 0.68 0.81 1.1 0.93 103 Q103M 0.89 1.06 0.76 0.99 0.9 1.01 103 Q103N 1.44 1.44 1.23 0.88 1.0 0.74 103 Q103R 1.09 0.47 0.57 0.88 1.1 1.04 103 Q103S 1.21 1.03 0.96 0.91 1.0 1.07 103 Q103T 0.84 1.01 0.94 0.95 1.0 0.89 103 Q103V 0.94 1.13 1.03 0.97 1.0 0.75 103 Q103W 0.98 0.65 0.63 0.73 1.1 0.76 104 Y104C 0.34 1.24 1.33 1.31 1.1 0.06 104 Y104F 0.90 0.88 0.78 1.03 1.0 0.67 104 Y104H 0.75 0.95 1.78 0.95 1.1 0.30 104 Y104I 0.30 1.10 1.10 1.48 1.3 0.08 104 Y104M 0.31 1.53 1.50 1.27 1.2 0.08 104 Y104N 0.46 1.42 1.78 1.04 1.1 0.10 104 Y104T 0.42 1.33 1.69 1.35 2.0 0.08 104 Y104W 0.62 0.82 0.89 1.17 1.2 1.38 105 S105A 0.67 1.06 0.97 1.01 1.0 1.16 105 S105C 0.32 0.91 1.10 0.81 1.1 0.52 105 S105D 0.39 1.33 1.03 1.21 1.1 0.90 105 S105E 0.54 0.98 0.79 0.93 1.2 0.76 105 S105G 0.68 1.12 0.98 0.98 0.9 0.93 105 S105I 0.19 1.60 1.06 0.72 1.0 0.26 105 S105K 0.21 0.13 0.10 0.13 1.2 0.09 105 S105L 0.17 0.60 9.45 0.53 1.2 0.12 105 S105M 0.18 1.09 1.67 1.11 0.9 0.19 105 S105N 0.32 1.10 0.97 1.17 1.1 0.81 105 S105Q 0.24 0.70 0.76 0.72 1.0 0.40 105 S105R 0.16 3.02 3.37 0.95 1.2 0.19 105 S105T 0.87 1.19 1.11 1.21 1.0 1.07 105 S105V 0.18 2.82 3.06 2.81 1.0 0.75 106 W106A 0.38 1.42 1.15 1.06 0.9 0.36 106 W106C 0.37 1.38 1.10 0.99 0.9 0.23 106 W106E 0.39 1.73 1.34 1.15 1.1 0.35 106 W106F 0.81 1.33 0.80 1.29 1.0 0.40 106 W106G 0.24 1.40 1.28 1.21 0.9 0.12 106 W106H 0.78 1.02 0.97 1.16 0.9 0.72 106 W106I 0.30 1.51 1.13 1.34 1.1 0.40 106 W106L 0.31 1.56 1.11 1.40 1.1 0.26 106 W106M 0.41 1.36 1.11 1.13 0.9 0.30 106 W106N 0.51 1.16 1.02 1.23 1.0 0.51 106 W106R 0.34 0.94 1.24 1.26 1.0 0.34 106 W106S 0.37 1.41 0.93 1.19 2.0 0.18 106 W106T 0.39 1.41 1.15 1.25 0.9 0.30 106 W106V 0.33 1.48 1.20 1.19 0.9 0.49 106 W106Y 0.90 1.19 1.05 1.22 0.9 0.43 107 I107E 0.47 1.07 1.99 1.00 1.0 0.95 107 I107F 0.54 0.87 0.79 1.16 1.0 0.06 107 I107L 0.84 0.57 0.33 0.48 1.0 0.95 107 I107M 0.86 1.18 2.50 0.93 1.0 0.17 107 I107R 0.23 2.33 2.34 1.86 1.2 0.06 107 I107S 0.46 1.41 0.88 1.22 1.0 0.08 107 I107T 0.70 1.35 2.33 0.93 1.0 0.13 107 I107V 0.82 0.71 0.73 0.78 0.9 1.33 108 I108A 0.38 1.15 1.22 1.17 0.8 0.70 108 I108C 0.79 1.09 1.19 1.00 0.9 0.76 108 I108E 0.21 0.23 1.19 0.59 0.9 0.13 108 I108L 0.73 1.29 1.29 1.05 1.0 0.41 108 I108M 0.80 1.10 1.21 1.10 0.7 0.73 108 I108Q 0.20 0.33 0.24 0.07 0.7 0.06 108 I108S 0.16 2.38 8.60 1.30 0.9 0.13 108 I108T 0.30 1.75 1.66 1.51 0.9 0.77 108 I108V 1.11 1.29 1.09 1.16 1.0 0.93 109 N109A 0.62 1.05 1.01 1.09 1.1 1.03 109 N109C 0.90 0.82 0.73 0.89 1.1 0.85 109 N109E 0.66 0.94 1.01 1.05 1.1 1.09 109 N109F 0.52 1.17 0.79 1.20 1.1 0.97 109 N109G 0.66 1.13 0.93 1.01 1.1 1.12 109 N109H 0.93 1.01 0.64 1.04 1.1 0.92 109 N109L 0.81 0.80 0.99 1.18 1.1 1.17 109 N109P 0.59 1.13 0.94 1.20 1.0 0.79 109 N109Q 1.04 0.63 0.55 0.99 1.2 0.93 109 N109R 0.71 0.58 0.57 1.03 1.0 1.07 109 N109S 1.03 0.93 0.90 1.13 1.0 1.05 109 N109T 0.94 1.26 0.82 1.02 0.9 1.09 109 N109V 0.59 0.91 0.91 1.17 1.0 1.08 109 N109W 0.63 0.92 0.76 1.15 0.9 0.92 109 N109Y 0.54 0.88 0.89 1.08 0.9 0.96 110 G110A 0.79 1.28 0.75 1.05 0.9 0.78 110 G110S 0.25 2.17 1.37 1.69 0.9 0.51 110 G110T 0.20 4.57 3.95 2.82 0.9 0.53 111 I111A 0.24 3.80 2.39 1.92 0.9 0.30 111 I111C 0.36 1.88 1.45 1.48 0.9 0.88 111 I111L 1.00 1.30 0.96 1.10 1.0 0.74 111 I111M 0.80 1.37 0.98 1.04 1.1 0.74 111 I111T 0.31 3.10 1.56 1.67 1.0 0.85 111 I111V 0.73 1.59 0.98 1.32 1.0 0.83 112 E112A 0.33 1.05 0.84 1.31 1.1 0.77 112 E112C 0.49 0.40 0.28 0.28 1.1 0.20 112 E112D 0.97 1.20 0.97 1.11 1.0 0.91 112 E112G 0.37 0.87 0.64 0.90 1.0 0.56 112 E112I 0.22 7.24 2.74 2.71 1.1 0.63 112 E112L 0.21 19.65 11.59 3.83 1.1 0.57 112 E112M 0.35 0.98 0.74 1.07 1.0 0.71 112 E112N 0.38 1.24 0.85 1.19 1.0 0.93 112 E112Q 0.39 1.25 1.01 1.27 1.0 0.97 112 E112S 0.38 1.22 0.98 1.05 1.0 0.85 112 E112T 0.25 2.89 2.14 1.98 1.0 0.90 113 W113C 0.19 0.36 1.25 1.25 1.0 0.19 113 W113D 0.18 0.52 1.67 0.60 0.9 0.16 113 W113E 0.19 0.26 1.58 0.31 0.9 0.16 113 W113F 0.50 0.97 1.02 1.03 0.9 0.96 113 W113H 0.22 1.45 1.69 1.49 1.1 0.57 113 W113M 0.19 0.40 1.19 0.61 0.9 0.18 113 W113N 0.17 0.74 2.31 0.88 0.9 0.22 113 W113T 0.17 0.12 1.00 0.51 1.1 0.10 113 W113Y 0.91 0.82 1.25 1.02 1.1 0.89 114 A114C 0.87 1.18 1.38 1.17 1.0 1.19 114 A114G 0.72 1.15 1.41 1.31 1.1 1.14 114 A114I 0.19 3.35 2.63 2.54 0.9 0.42 114 A114S 0.33 1.15 1.39 1.63 1.0 0.98 114 A114T 0.59 1.03 1.49 1.53 0.9 1.46 114 A114V 0.31 1.57 2.18 1.56 0.9 0.97 115 I115A 0.40 1.58 0.99 1.09 0.9 0.79 115 I115C 0.69 1.23 0.81 1.25 1.0 1.10 115 I115E 0.28 2.29 1.67 1.56 0.9 0.69 115 I115F 0.30 1.99 1.22 1.37 0.9 0.61 115 I115H 0.24 4.85 2.46 2.39 0.9 0.52 115 I115L 0.83 1.04 0.96 1.08 1.1 1.06 115 I115M 0.89 1.46 1.03 1.09 1.0 0.94 115 I115N 0.21 8.31 8.40 2.63 1.0 0.37 115 I115Q 0.58 1.30 0.80 1.24 1.0 1.00 115 I115R 0.38 1.37 1.00 1.21 1.0 0.86 115 I115S 0.24 4.20 2.44 2.22 0.9 0.70 115 I115T 0.59 1.46 0.89 1.08 0.9 0.91 115 I115V 0.84 1.44 0.99 1.25 0.9 1.58 115 I115Y 0.24 4.81 4.07 2.48 0.9 0.79 116 A116C 1.15 0.85 1.06 0.90 1.0 0.95 116 A116D 1.24 1.02 0.81 1.03 1.0 1.11 116 A116E 1.16 1.21 1.09 0.89 1.0 1.08 116 A116F 0.95 1.06 0.92 0.94 1.0 1.01 116 A116G 0.66 0.94 1.01 0.97 1.0 1.08 116 A116H 1.07 1.09 0.92 1.13 1.0 1.30 116 A116I 0.95 0.82 1.04 1.13 1.0 1.05 116 A116K 1.18 0.74 0.79 1.13 1.0 0.94 116 A116L 0.82 1.05 0.89 0.83 1.0 0.98 116 A116M 1.11 0.86 1.14 0.85 1.0 0.98 116 A116N 0.99 0.97 0.88 1.10 1.0 1.15 116 A116Q 1.07 0.85 0.71 1.03 1.0 1.15 116 A116R 1.15 0.86 0.73 1.09 1.0 1.15 116 A116S 1.14 1.07 0.98 1.17 0.9 1.11 116 A116T 1.03 1.01 1.12 1.06 0.9 1.17 116 A116V 0.88 1.03 1.03 0.96 1.0 1.09 116 A116W 0.86 1.24 0.71 0.97 1.0 1.17 116 A116Y 0.88 0.89 1.03 0.93 0.9 1.19 117 N117C 0.60 1.00 0.98 1.07 1.0 1.06 117 N117E 0.52 0.97 1.03 1.06 1.0 1.18 117 N117F 0.40 1.04 1.21 1.17 0.9 1.33 117 N117G 0.67 1.18 0.85 1.29 1.1 0.96 117 N117K 0.22 1.91 1.91 1.80 1.0 0.88 117 N117L 0.30 1.13 1.22 1.39 1.0 1.13 117 N117M 0.57 1.09 1.21 1.12 1.0 1.24 117 N117Q 1.04 0.69 0.95 0.99 1.1 1.10 117 N117R 0.80 0.98 0.78 0.98 1.0 0.90 117 N117S 0.53 1.18 1.24 1.06 1.3 1.14 117 N117T 0.80 1.05 1.07 1.15 1.0 1.13 117 N117V 0.17 5.36 4.11 2.10 1.0 0.46 117 N117W 0.25 2.09 1.77 1.63 1.0 1.05 117 N117Y 0.45 0.99 0.89 1.22 1.0 0.98 118 N118A 0.71 0.58 0.84 0.95 1.0 1.14 118 N118C 0.74 0.61 1.01 0.63 1.1 0.94 118 N118D 1.12 0.67 1.05 0.86 1.2 1.01 118 N118E 0.88 0.71 0.70 0.69 1.1 1.16 118 N118F 0.34 1.02 1.31 0.93 1.0 1.07 118 N118G 1.07 0.83 0.50 0.79 0.9 0.92 118 N118H 1.18 0.75 0.88 0.92 1.0 1.07 118 N118I 0.17 4.85 5.90 1.96 1.1 0.62 118 N118K 1.17 0.80 0.81 0.81 1.1 0.95 118 N118L 0.23 1.45 1.85 1.32 1.0 1.13 118 N118M 0.49 0.87 0.99 1.06 1.0 1.17 118 N118Q 1.03 0.62 1.12 0.90 1.1 1.09 118 N118R 1.35 0.82 0.62 0.80 1.0 1.01 118 N118S 0.89 0.77 0.81 0.76 0.9 1.07 118 N118T 0.64 0.72 0.86 1.08 0.9 1.21 118 N118V 0.23 1.35 1.92 1.53 1.0 0.99 118 N118W 0.27 1.16 1.36 1.41 1.1 1.03 118 N118Y 0.84 0.98 0.72 0.70 1.0 1.13 119 M119A 0.75 1.01 1.16 1.01 0.8 0.85 119 M119C 0.86 1.01 1.16 0.95 1.0 0.99 119 M119F 0.29 1.64 1.87 1.60 1.3 0.78 119 M119G 0.26 0.33 0.48 0.28 1.0 0.11 119 M119H 0.30 1.19 1.46 1.22 1.1 0.67 119 M119I 0.74 1.20 1.16 0.94 1.1 0.97 119 M119L 0.65 1.17 1.19 0.82 1.0 0.98 119 M119N 0.23 1.95 2.59 1.79 1.1 0.83 119 M119S 0.53 1.19 1.30 0.87 0.8 1.04 119 M119T 0.46 1.25 1.32 1.03 1.0 1.43 119 M119V 0.75 0.95 1.13 0.91 0.7 1.14 120 D120A 1.01 1.11 0.84 0.80 1.0 0.85 120 D120C 0.67 0.84 0.95 0.76 1.0 0.92 120 D120E 1.04 0.60 0.87 1.04 1.1 0.99 120 D120F 0.24 0.50 1.07 0.78 1.0 0.50 120 D120G 1.00 0.99 1.04 0.97 0.8 0.92 120 D120H 1.13 1.07 1.16 0.88 1.1 0.93 120 D120I 0.20 0.92 1.69 1.26 1.0 0.55 120 D120K 1.15 0.88 1.01 0.95 1.1 0.81 120 D120L 0.33 0.65 1.25 1.12 1.1 0.88 120 D120M 0.73 0.87 0.97 0.95 0.7 0.93 120 D120N 1.11 1.01 1.00 0.92 1.1 0.90 120 D120P 0.22 1.12 1.61 1.14 1.1 0.53 120 D120Q 1.05 1.21 1.09 0.96 1.1 0.87 120 D120R 1.03 0.86 0.97 1.10 0.9 0.93 120 D120S 1.01 0.94 1.16 0.86 1.0 0.97 120 D120T 0.77 1.08 1.09 1.00 1.0 1.06 120 D120V 0.32 1.13 1.21 0.64 1.1 0.81 120 D120W 0.32 1.10 1.44 1.19 1.1 0.95 120 D120Y 0.22 1.30 1.73 1.29 1.0 0.70 121 V121C 0.76 0.98 0.99 0.78 1.1 0.92 121 V121E 0.19 0.45 1.16 0.85 0.7 0.21 121 V121F 0.18 0.12 1.14 0.47 0.7 0.12 121 V121I 1.15 0.83 0.88 0.81 1.0 0.89 121 V121L 0.81 0.95 0.91 0.88 0.8 0.94 121 V121T 0.26 1.28 1.66 1.24 1.1 0.85 122 I122A 0.92 1.06 1.04 1.00 0.8 0.88 122 I122C 0.78 1.17 1.22 1.09 0.8 0.98 122 I122F 0.37 1.16 1.45 1.19 1.4 0.66 122 I122L 0.73 0.99 1.28 1.09 0.8 0.97 122 I122M 0.93 1.17 1.05 1.23 0.8 0.96 122 I122S 0.22 6.46 6.12 2.56 1.9 0.43 122 I122T 0.34 1.78 1.79 1.13 1.4 0.90 122 I122V 0.80 1.14 1.39 1.13 0.7 1.09 123 N123C 0.95 1.53 1.35 1.43 0.5 0.09 123 N123G 0.47 1.81 1.59 1.34 0.4 0.13 123 N123Q 0.87 1.22 1.30 1.03 0.7 0.09 123 N123S 0.92 1.31 1.15 1.08 0.2 0.09 123 N123T 0.94 1.20 1.41 0.93 0.4 0.13 124 M124A 0.61 1.44 1.02 0.97 1.0 0.69 124 M124C 0.26 0.86 0.54 0.63 1.3 0.07 124 M124F 1.13 1.02 0.86 1.06 0.9 0.34 124 M124I 1.36 1.12 1.08 1.12 1.0 0.34 124 M124L 0.86 0.69 1.01 1.03 1.2 0.92 124 M124S 0.28 2.79 1.44 1.52 0.9 0.12 124 M124T 0.49 1.82 1.32 1.35 0.9 0.23 124 M124V 1.07 1.37 1.15 1.06 0.9 0.31 125 S125A 0.92 1.90 1.40 1.17 1.1 0.06 126 L126I 1.11 1.17 1.03 1.17 1.1 0.11 126 L126V 1.09 1.26 1.34 1.32 1.0 0.08 126 L126W 0.89 0.71 0.79 0.78 0.9 0.06 128 G128A 1.21 1.24 1.28 1.21 1.0 0.16 128 G128S 1.35 1.17 1.12 1.09 1.2 0.26 129 P129A 1.04 1.02 0.98 0.99 0.7 0.80 129 P129C 1.37 1.09 1.11 0.91 0.9 0.56 129 P129D 1.48 1.03 1.08 0.84 1.1 0.67 129 P129E 1.42 1.24 1.04 1.10 1.0 0.87 129 P129F 0.65 1.10 0.71 1.00 0.7 1.27 129 P129G 0.78 0.82 0.60 0.81 0.8 0.56 129 P129H 0.66 0.92 0.73 0.84 0.9 0.81 129 P129I 1.14 0.95 0.99 1.11 0.9 0.40 129 P129K 1.13 0.72 0.64 1.01 0.9 1.22 129 P129L 1.12 1.13 1.21 1.06 0.9 0.53 129 P129M 1.20 1.08 0.92 1.20 0.9 0.88 129 P129N 0.90 1.00 1.04 0.98 0.9 0.85 129 P129Q 1.10 1.22 0.90 1.01 1.0 0.98 129 P129R 0.74 0.73 0.75 0.87 0.9 1.01 129 P129S 1.07 0.99 0.87 0.98 0.9 0.84 129 P129T 1.13 1.29 1.17 1.09 0.9 1.06 129 P129V 0.72 1.41 1.26 1.09 0.8 0.75 129 P129W 0.38 0.97 0.79 1.18 0.4 1.18 129 P129Y 0.71 1.01 0.90 1.04 0.8 1.56 130 S130A 1.14 0.92 0.76 0.86 1.0 0.92 130 S130C 1.24 0.75 0.95 0.66 1.1 0.78 130 S130E 1.36 0.73 1.29 1.03 1.1 0.88 130 S130F 1.17 0.89 0.79 0.84 1.0 1.02 130 S130G 0.93 0.95 0.99 0.98 0.9 0.80 130 S130H 1.33 0.76 0.97 1.05 1.1 1.03 130 S130I 1.22 0.82 0.97 0.91 1.1 0.95 130 S130K 1.27 0.63 0.70 0.67 1.1 1.12 130 S130L 1.04 0.90 0.79 0.80 1.1 0.98 130 S130M 1.19 0.97 0.91 0.89 0.9 0.92 130 S130P 0.60 1.32 1.32 1.00 0.7 0.07 130 S130Q 1.19 0.98 0.95 0.93 1.1 1.06 130 S130R 1.12 0.47 0.63 0.77 1.1 1.11 130 S130T 1.16 1.08 1.10 0.95 0.9 1.19 130 S130V 1.13 0.98 0.96 0.91 1.0 1.07 130 S130W 0.73 0.60 0.81 0.86 0.8 0.89 130 S130Y 1.24 0.73 0.94 0.95 1.0 1.04 131 G131A 1.21 0.53 1.00 0.84 1.1 1.02 131 G131C 0.55 0.59 0.82 0.83 0.6 0.87 131 G131D 0.93 0.50 0.80 0.78 0.9 1.32 131 G131F 0.23 0.42 0.55 0.67 0.2 0.43 131 G131K 1.00 0.48 1.00 0.89 1.0 1.39 131 G131M 0.53 0.47 0.89 0.75 0.6 0.90 131 G131N 0.46 0.23 0.49 0.54 0.8 1.11 131 G131P 0.22 0.77 1.29 1.21 0.1 0.50 131 G131Q 0.28 0.49 1.15 0.95 0.3 0.70 131 G131R 0.19 0.97 2.04 1.64 0.1 0.59 131 G131S 0.21 0.12 0.47 0.83 0.2 0.45 131 G131T 0.86 0.52 1.16 0.89 1.0 1.03 131 G131V 0.51 0.50 0.83 0.94 0.7 0.99 131 G131Y 0.30 0.26 0.40 0.71 0.9 1.04 132 S132A 0.60 1.01 1.03 1.03 0.5 0.77 132 S132C 1.25 1.06 1.10 0.83 1.0 0.64 132 S132E 0.33 1.04 1.40 1.01 0.9 0.50 132 S132G 0.83 0.83 0.14 0.94 1.0 0.41 132 S132I 0.25 1.62 1.82 1.25 0.8 0.57 132 S132K 0.19 0.09 0.60 0.16 0.7 0.11 132 S132L 0.25 1.27 1.65 1.22 0.8 0.78 132 S132M 0.35 1.01 1.05 1.05 0.6 0.72 132 S132N 0.88 1.38 1.35 1.17 1.0 0.87 132 S132P 0.17 9.36 11.70 2.50 1.0 0.23 132 S132Q 0.34 1.35 1.28 1.18 0.7 0.88 132 S132V 0.23 3.29 2.39 2.07 0.8 0.58 133 A133C 0.98 0.87 1.06 0.79 1.1 0.84 133 A133D 0.91 0.90 0.79 0.81 1.0 0.62 133 A133E 1.07 0.93 0.96 0.84 1.0 0.99 133 A133F 0.83 0.95 0.65 0.93 0.9 1.11 133 A133G 0.78 0.95 0.95 0.92 1.0 1.12 133 A133I 0.95 0.88 0.88 0.84 1.0 1.49 133 A133K 1.11 0.75 0.65 0.72 1.1 1.02 133 A133L 0.93 0.78 0.83 0.88 1.0 1.15 133 A133M 0.95 0.99 0.71 0.85 1.0 1.00 133 A133P 1.10 1.21 0.74 0.83 1.2 0.94 133 A133Q 0.85 1.25 0.98 0.79 1.1 1.07 133 A133R 0.93 0.51 0.41 0.65 1.1 0.97 133 A133S 1.05 1.00 0.94 0.82 1.0 1.06 133 A133T 0.96 1.03 0.78 0.82 1.1 1.14 133 A133V 0.98 0.95 0.89 0.87 1.1 1.07 133 A133W 0.73 0.86 0.42 0.73 1.1 1.09 133 A133Y 0.84 0.71 0.75 0.65 1.1 1.12 134 A134C 0.78 0.83 1.13 0.80 1.0 0.82 134 A134F 0.26 0.99 0.97 0.88 0.9 0.86 134 A134G 0.63 1.14 0.59 0.93 1.2 0.74 134 A134I 0.26 1.60 1.22 1.29 0.9 0.93 134 A134L 0.19 1.85 2.41 1.75 1.1 0.61 134 A134M 0.21 1.40 1.20 1.29 1.1 0.53 134 A134P 0.78 1.06 0.86 0.95 1.0 1.25 134 A134Q 0.19 0.12 0.36 0.32 1.1 0.10 134 A134S 0.97 1.04 0.91 0.92 1.1 1.12 134 A134T 0.94 1.03 0.86 1.04 1.0 1.04 134 A134V 0.39 1.27 1.04 0.84 0.9 1.14 135 L135A 0.23 1.24 0.90 1.12 1.0 0.07 135 L135E 0.43 1.19 1.03 0.88 1.1 0.82 135 L135I 0.34 1.41 0.97 1.06 0.7 0.16 135 L135M 1.03 1.01 1.19 0.96 1.1 0.59 135 L135T 0.19 3.36 2.29 2.06 0.6 0.06 135 L135V 0.34 2.12 1.12 1.33 0.6 0.19 135 L135W 0.27 2.14 1.96 1.47 0.8 0.23 136 K136A 0.57 0.80 1.04 0.83 0.9 0.80 136 K136C 0.51 1.02 1.04 0.74 0.9 0.81 136 K136D 0.21 1.62 1.47 0.92 0.4 0.47 136 K136E 1.03 0.92 0.73 0.82 1.2 1.03 136 K136F 0.27 1.35 1.57 1.15 0.6 0.82 136 K136G 0.44 1.09 1.12 0.91 0.7 0.82 136 K136H 0.89 0.99 1.00 0.68 1.1 1.08 136 K136I 0.20 2.18 2.48 1.44 0.4 0.47 136 K136L 0.65 1.05 0.71 0.90 1.0 1.16 136 K136M 0.69 1.02 0.87 0.87 0.9 1.09 136 K136N 0.60 1.08 0.88 0.81 1.0 0.88 136 K136R 0.82 1.02 0.82 0.69 1.1 1.01 136 K136S 0.39 1.08 0.87 0.92 0.7 0.80 136 K136V 0.21 2.18 2.41 1.96 0.5 0.83 136 K136W 0.44 1.03 0.93 0.80 0.6 0.91 136 K136Y 0.25 1.78 1.41 1.21 0.4 0.94 137 A137C 1.00 0.91 0.95 0.71 1.1 1.08 137 A137D 1.14 1.04 1.00 0.81 1.0 1.06 137 A137E 0.75 0.91 1.10 0.88 1.1 1.03 137 A137F 0.59 1.01 0.78 0.90 1.0 1.41 137 A137G 0.72 1.01 0.91 0.78 1.1 1.24 137 A137H 1.02 0.95 0.78 0.91 0.9 1.03 137 A137K 0.90 0.96 0.52 0.90 1.0 1.17 137 A137L 0.84 0.85 0.82 0.89 1.1 1.07 137 A137M 0.93 1.09 0.89 0.85 1.0 1.06 137 A137N 1.01 1.02 0.62 0.77 1.0 1.38 137 A137P 0.18 3.85 3.42 1.76 0.2 0.10 137 A137Q 1.05 1.05 0.60 0.92 1.0 1.18 137 A137R 0.65 0.65 0.49 0.70 1.0 1.17 137 A137S 0.98 0.91 0.92 1.08 0.9 1.11 137 A137T 0.96 0.94 0.77 0.96 1.0 1.07 137 A137V 0.62 1.27 0.85 1.06 0.8 1.23 137 A137W 0.69 0.81 0.55 0.62 0.9 1.50 137 A137Y 0.83 1.05 0.73 0.66 0.9 1.33 138 A138C 0.85 1.04 1.10 1.14 0.9 1.07 138 A138D 0.17 1.47 4.55 2.27 0.3 0.16 138 A138E 0.36 1.44 0.96 1.13 0.9 0.83 138 A138F 0.18 2.55 2.71 1.96 0.8 0.31 138 A138G 0.52 1.27 1.35 1.07 0.9 1.16 138 A138H 0.20 2.04 2.24 1.84 0.7 0.52 138 A138I 0.78 0.93 0.98 1.11 0.9 1.18 138 A138L 0.27 1.23 1.19 1.42 0.9 0.70 138 A138M 0.71 0.88 0.89 1.00 1.0 0.91 138 A138Q 0.17 11.86 16.19 4.99 0.9 0.75 138 A138S 0.86 1.05 0.99 1.02 0.7 1.22 138 A138T 0.51 1.17 1.27 1.18 0.9 1.07 138 A138V 0.76 1.08 1.11 1.05 0.9 1.12 138 A138Y 0.17 5.98 9.05 3.30 0.6 0.51 139 V139A 0.69 1.06 1.06 0.97 0.8 0.94 139 V139C 1.19 1.03 1.09 0.95 1.0 1.30 139 V139G 0.21 0.40 0.60 0.65 0.5 0.25 139 V139H 0.25 0.75 0.74 0.73 0.8 0.06 139 V139I 0.85 0.84 0.73 1.02 1.0 0.43 139 V139L 0.75 0.98 0.84 1.09 0.8 0.28 139 V139M 0.61 0.97 0.67 1.01 0.6 0.49 139 V139N 0.47 0.83 0.76 1.14 0.9 1.20 139 V139S 0.49 0.78 1.11 1.11 0.9 0.98 139 V139T 0.42 1.27 0.83 1.19 1.0 0.63 140 D140A 0.45 0.70 0.72 0.81 0.2 0.61 140 D140C 0.56 0.90 1.02 0.89 0.8 0.88 140 D140E 1.02 1.20 0.98 0.92 0.9 1.01 140 D140G 0.52 0.80 0.79 0.85 0.7 0.86 140 D140H 0.50 0.47 0.53 0.67 0.7 0.72 140 D140K 0.48 0.25 0.53 0.47 0.8 0.85 140 D140L 0.42 0.54 0.78 0.84 0.1 0.97 140 D140M 0.48 0.77 0.81 0.82 0.3 0.95 140 D140N 0.88 0.86 0.84 0.83 0.9 0.97 140 D140Q 0.61 0.87 0.80 0.96 0.7 1.31 140 D140R 0.41 0.22 0.28 0.50 0.7 0.98 140 D140S 0.55 0.81 0.77 0.92 0.4 0.83 140 D140T 0.60 0.85 0.80 0.89 0.5 0.87 140 D140V 0.42 0.98 1.00 0.96 0.2 1.07 140 D140W 0.23 0.74 0.78 0.85 0.4 0.95 140 D140Y 0.50 0.79 0.74 0.83 0.6 1.05 141 K141A 0.87 0.87 1.11 0.93 1.0 1.06 141 K141C 0.78 0.73 1.11 1.04 1.0 1.11 141 K141D 0.82 0.95 1.23 1.04 1.0 1.14 141 K141E 1.18 0.80 1.10 1.00 1.0 0.97 141 K141F 0.70 0.84 1.27 1.04 1.0 1.13 141 K141G 0.94 0.84 1.15 1.07 1.1 1.09 141 K141H 1.00 1.03 1.09 1.04 1.2 1.08 141 K141I 0.60 0.94 1.23 1.00 1.1 1.25 141 K141L 0.66 0.87 1.29 1.01 1.1 1.14 141 K141M 0.79 1.00 1.17 1.02 1.0 1.24 141 K141N 1.05 0.90 1.30 1.03 1.1 1.17 141 K141Q 1.06 0.96 1.26 1.09 1.1 1.10 141 K141R 1.09 0.87 1.13 1.07 1.0 0.97 141 K141S 0.95 0.96 1.06 1.22 1.0 1.15 141 K141V 0.60 1.20 1.28 1.02 1.0 1.36 141 K141W 0.70 1.14 1.32 1.18 1.2 1.27 141 K141Y 0.91 1.16 1.07 1.06 1.1 1.16 142 A142C 0.79 1.03 0.92 0.89 1.1 1.17 142 A142G 0.46 1.32 1.20 0.96 1.0 1.18 142 A142I 0.25 1.60 1.39 1.46 0.6 0.81 142 A142L 0.29 1.24 1.40 1.19 0.6 0.70 142 A142M 0.22 1.21 1.62 1.31 0.6 0.38 142 A142S 0.68 1.01 0.98 1.23 1.0 1.18 142 A142T 0.31 1.32 1.55 1.46 0.8 1.11 142 A142V 0.37 1.49 1.19 1.23 0.8 1.12 143 V143A 1.05 0.81 1.04 0.90 0.9 0.88 143 V143C 0.87 1.00 1.14 0.89 1.0 1.08 143 V143D 0.95 0.95 1.03 0.97 1.0 1.05 143 V143E 1.12 0.87 1.05 1.02 1.0 1.08 143 V143F 0.88 0.76 1.00 0.81 0.9 0.81 143 V143G 0.71 0.90 1.16 1.15 0.9 1.11 143 V143K 0.84 0.61 0.72 0.96 1.1 1.00 143 V143L 0.78 0.78 1.13 0.83 0.9 1.11 143 V143M 0.83 0.94 1.05 1.11 0.9 0.99 143 V143N 0.91 0.90 1.00 1.20 1.0 1.13 143 V143Q 0.88 0.82 1.11 1.04 1.1 1.04 143 V143R 0.77 0.64 0.70 0.92 1.0 0.94 143 V143S 1.03 0.94 0.97 0.93 1.0 1.02 143 V143T 0.83 0.90 0.93 0.99 1.0 1.17 143 V143W 0.65 1.36 0.84 1.02 0.9 0.88 144 A144C 1.17 0.98 0.85 0.88 1.0 1.02 144 A144D 1.29 1.18 1.11 0.99 1.0 0.96 144 A144E 1.17 1.08 0.76 1.00 1.0 1.13 144 A144F 0.96 1.20 0.73 0.94 1.0 1.16 144 A144G 1.09 1.08 0.98 1.02 1.0 0.99 144 A144I 0.97 1.29 0.79 0.97 1.1 1.06 144 A144K 1.28 1.00 0.57 0.77 1.1 0.90 144 A144L 1.11 1.18 0.79 1.08 1.0 1.03 144 A144M 1.06 1.08 0.84 1.07 1.0 1.05 144 A144P 0.18 1.75 2.60 1.24 0.4 0.30 144 A144R 1.23 0.96 0.45 0.90 1.1 1.00 144 A144S 1.04 1.24 0.93 0.85 1.0 1.05 144 A144T 1.08 1.16 0.89 1.04 1.1 1.14 144 A144V 0.80 1.11 1.13 0.86 1.0 1.21 144 A144W 0.87 1.23 0.64 0.88 1.0 1.63 145 S145A 1.09 0.97 1.13 0.94 1.0 0.99 145 S145C 1.10 0.72 1.03 1.00 1.1 1.03 145 S145D 1.24 1.03 1.06 1.08 1.1 1.01 145 S145E 1.24 0.90 1.20 0.90 1.1 0.95 145 S145F 0.84 0.81 1.15 1.12 1.1 1.22 145 S145G 1.06 0.77 1.13 1.06 1.0 1.11 145 S145H 1.21 0.93 1.04 1.05 1.1 1.02 145 S145I 0.79 0.42 1.24 1.03 1.1 1.24 145 S145L 0.87 1.02 1.25 1.08 1.1 1.13 145 S145M 1.00 0.86 1.06 1.04 1.0 1.08 145 S145Q 1.10 0.74 1.18 1.08 1.0 1.06 145 S145R 1.21 0.78 1.01 1.13 1.1 1.06 145 S145T 1.04 0.92 1.17 1.04 1.0 1.07 145 S145V 0.83 0.87 1.25 1.06 1.0 1.17 145 S145W 0.81 1.15 1.10 1.01 0.9 1.21 145 S145Y 0.48 0.88 1.28 1.13 0.9 1.29 146 G146A 0.48 1.04 1.18 1.08 1.0 1.02 146 G146C 0.50 1.01 1.15 0.98 1.1 0.97 146 G146D 1.08 0.86 1.02 1.00 1.1 1.07 146 G146E 0.82 0.79 1.12 0.98 1.0 1.04 146 G146F 0.50 0.88 1.03 1.06 1.0 1.02 146 G146H 0.92 0.86 1.17 1.06 0.9 1.09 146 G146K 0.89 0.72 1.09 0.98 0.9 1.07 146 G146L 0.18 2.22 3.81 1.88 1.1 0.59 146 G146M 0.34 1.18 1.21 1.22 1.0 1.09 146 G146P 0.18 0.49 0.60 0.25 0.2 0.08 146 G146Q 0.85 0.95 1.16 1.05 1.0 1.45 146 G146R 0.81 0.79 1.08 1.04 0.9 1.02 146 G146S 0.76 0.92 1.11 0.91 0.9 1.06 146 G146T 0.25 1.52 1.80 1.57 0.7 1.12 146 G146Y 0.21 1.66 2.23 1.62 0.9 0.88 147 V147A 1.13 1.04 1.09 0.92 1.1 0.90 147 V147C 0.87 1.19 1.25 0.99 1.1 0.90 147 V147D 0.21 2.29 3.05 2.09 1.2 0.53 147 V147E 0.53 0.98 1.17 0.93 1.0 1.12 147 V147G 0.64 1.25 1.42 1.04 1.0 0.93 147 V147H 0.70 1.23 1.30 0.94 1.2 0.93 147 V147I 0.98 1.25 0.94 0.94 1.1 1.04 147 V147L 0.70 1.16 1.29 1.15 1.0 0.97 147 V147M 0.97 1.00 1.07 0.90 1.0 1.14 147 V147P 0.31 1.71 2.12 1.52 0.8 1.13 147 V147Q 0.84 1.23 1.09 1.03 1.2 1.01 147 V147R 0.71 1.16 1.07 0.88 1.0 0.96 147 V147S 0.87 1.06 1.22 0.87 1.0 0.98 147 V147T 0.80 1.24 1.06 1.02 0.9 1.16 147 V147W 0.25 1.97 2.16 1.32 0.9 0.93 147 V147Y 0.26 2.34 2.31 1.50 0.9 0.78 148 V148A 0.56 1.06 0.76 1.03 0.8 0.74 148 V148E 0.21 0.62 0.99 0.67 0.9 0.14 148 V148F 0.73 0.96 1.18 1.06 0.9 0.85 148 V148G 0.23 0.70 1.12 0.98 0.9 0.26 148 V148H 0.30 1.07 1.68 1.39 0.8 0.74 148 V148I 0.70 0.98 1.20 1.02 1.1 0.91 148 V148L 0.98 1.05 1.11 1.07 1.1 0.80 148 V148M 0.64 0.94 1.06 1.01 0.8 0.74 148 V148N 0.41 1.38 1.35 1.11 0.8 1.11 148 V148P 0.27 0.61 0.87 0.76 1.0 0.21 148 V148Q 0.25 1.08 1.73 1.58 1.0 0.82 148 V148S 0.52 1.09 1.20 1.10 1.0 0.90 148 V148T 0.55 1.05 1.41 1.13 1.0 0.99 148 V148Y 0.22 1.60 1.45 1.60 0.6 0.37 149 V149A 0.80 0.96 1.10 0.99 1.0 0.99 149 V149C 0.86 1.11 0.96 0.99 1.2 0.89 149 V149D 0.22 0.83 1.23 1.11 1.3 0.32 149 V149E 0.18 2.65 3.71 2.50 1.0 0.40 149 V149F 0.92 1.15 1.31 1.07 1.0 0.23 149 V149G 0.24 0.90 0.72 1.05 1.0 0.28 149 V149H 0.25 0.54 0.75 0.70 1.2 0.26 149 V149I 0.84 0.96 1.08 0.85 1.1 0.80 149 V149L 0.69 1.02 1.11 1.11 1.1 0.98 149 V149M 0.82 1.09 1.11 1.07 1.1 0.82 149 V149P 0.46 0.94 1.23 1.04 1.2 1.25 149 V149S 0.37 1.12 1.42 1.31 1.1 1.18 149 V149T 0.66 0.88 1.16 1.09 1.1 1.11 149 V149W 0.25 0.44 0.50 0.59 1.3 0.12 149 V149Y 0.33 1.18 1.52 1.33 1.0 0.18 150 V150A 0.54 0.85 1.21 1.04 0.9 0.67 150 V150C 0.80 0.86 1.07 1.06 1.0 0.80 150 V150F 0.47 0.89 1.07 1.07 0.8 0.86 150 V150I 0.83 1.14 1.05 1.07 1.0 1.15 150 V150L 0.75 0.97 0.96 1.02 0.9 0.95 150 V150M 0.39 0.97 1.26 1.27 0.9 0.77 150 V150N 0.28 0.27 0.26 0.21 1.1 0.06 150 V150Q 0.31 1.25 1.67 1.46 1.0 1.05 150 V150S 0.33 1.08 1.22 1.17 0.8 0.52 150 V150T 0.61 0.71 1.28 1.09 1.0 0.72 151 A151C 0.74 1.20 0.94 0.98 0.9 0.91 151 A151G 0.49 0.85 1.24 1.16 0.8 0.74 151 A151M 0.24 1.15 1.42 1.13 1.0 0.32 151 A151N 0.21 0.93 1.88 1.11 0.7 0.13 151 A151S 0.79 0.96 1.26 1.08 1.0 0.51 151 A151T 0.46 1.36 1.20 1.18 0.6 0.56 151 A151V 0.38 0.95 1.08 1.45 0.6 0.61 152 A152S 1.11 0.74 1.00 0.85 0.9 0.32 153 A153C 0.54 1.02 1.03 0.96 0.5 0.67 153 A153G 0.51 1.03 1.06 1.03 0.5 0.64 153 A153S 0.65 1.05 1.03 1.04 0.6 0.62 153 A153V 0.28 1.34 1.24 1.39 0.3 0.88 154 G154S 0.22 0.58 0.78 0.76 0.2 0.06 156 E156A 1.12 0.69 0.60 0.84 1.0 0.87 156 E156C 1.10 0.61 0.70 0.83 1.0 0.85 156 E156F 1.11 0.41 0.57 0.89 1.0 1.12 156 E156I 0.43 0.59 0.64 0.86 0.5 0.86 156 E156K 0.99 0.42 0.41 0.78 0.5 1.30 156 E156L 0.82 0.55 0.60 0.83 0.8 1.31 156 E156M 1.10 0.46 0.57 0.86 0.9 1.31 156 E156N 1.17 0.38 0.48 0.72 1.0 0.91 156 E156Q 0.93 0.51 0.51 0.75 0.9 0.94 156 E156R 1.10 0.23 0.41 0.66 0.4 1.35 156 E156S 0.93 0.62 0.52 0.91 0.8 1.01 156 E156T 0.72 0.73 0.65 1.00 0.7 1.44 156 E156V 0.54 0.60 0.60 0.98 0.6 1.13 156 E156W 0.79 0.24 0.21 0.60 0.7 0.79 156 E156Y 1.10 0.35 0.43 0.72 0.9 1.09 157 G157A 0.48 0.83 0.87 0.92 0.6 0.62 157 G157C 0.60 0.63 0.79 0.95 0.4 0.18 157 G157D 0.49 0.68 0.87 0.79 0.4 0.20 157 G157E 0.58 0.62 0.82 0.69 0.2 0.12 157 G157F 0.34 0.38 0.60 0.68 0.2 0.19 157 G157I 0.34 0.34 0.53 0.54 0.1 0.06 157 G157L 0.40 0.33 0.54 0.60 0.1 0.06 157 G157M 0.43 0.58 0.72 0.66 0.2 0.11 157 G157P 0.45 0.32 0.42 0.58 0.1 0.09 157 G157Q 0.41 0.55 0.80 0.71 0.2 0.13 157 G157R 0.31 0.28 0.52 0.43 0.1 0.15 157 G157S 0.53 1.03 0.96 0.88 0.8 0.72 157 G157T 0.37 0.51 0.81 0.97 0.2 0.12 157 G157V 0.33 0.43 0.74 0.63 0.1 0.09 157 G157W 0.40 0.59 0.70 0.88 0.2 0.18 157 G157Y 0.29 0.74 0.80 0.80 0.3 0.27 158 T158A 0.94 0.98 0.98 0.92 0.8 1.10 158 T158D 0.68 1.09 1.09 1.04 1.1 0.94 158 T158E 1.10 1.09 1.03 0.98 1.2 0.95 158 T158G 0.77 1.11 0.47 1.06 0.8 0.75 158 T158H 0.85 1.04 0.95 0.92 0.9 0.87 158 T158I 1.02 1.08 0.75 0.91 1.0 0.96 158 T158K 0.83 1.05 0.53 0.85 0.8 0.97 158 T158L 0.71 1.06 0.65 0.83 0.8 0.73 158 T158M 0.80 0.97 0.71 0.97 0.7 0.71 158 T158N 0.79 1.16 0.69 0.85 1.0 0.80 158 T158P 0.58 1.12 0.88 0.86 0.7 0.66 158 T158Q 0.82 1.04 0.89 0.81 1.0 0.81 158 T158R 0.56 0.84 0.54 0.83 0.5 1.02 158 T158S 1.31 1.09 1.04 0.93 0.9 0.94 158 T158V 0.93 1.20 0.83 0.86 0.9 0.95 158 T158W 0.61 1.01 0.75 0.89 0.6 0.82 158 T158Y 0.75 1.01 0.53 1.04 0.7 0.84 159 S159A 0.92 0.93 0.90 1.07 0.7 0.78 159 S159C 1.16 1.08 1.18 0.87 1.1 0.93 159 S159D 1.41 1.26 1.15 1.05 1.1 0.92 159 S159E 1.07 1.04 1.13 1.07 1.0 0.90 159 S159F 0.73 1.14 0.93 1.06 0.4 0.74 159 S159G 0.88 1.14 1.13 0.91 0.6 0.86 159 S159H 1.10 0.95 0.85 0.88 1.0 1.05 159 S159I 0.90 1.03 1.02 0.92 0.4 0.63 159 S159K 1.24 1.37 0.92 1.00 1.0 1.08 159 S159L 0.77 1.09 1.15 1.25 0.4 0.77 159 S159M 0.81 1.02 1.22 0.92 0.5 0.70 159 S159P 0.72 1.20 0.94 1.05 0.3 0.62 159 S159Q 1.10 1.06 1.16 1.11 1.1 1.08 159 S159R 1.09 0.78 0.87 0.93 0.9 1.07 159 S159T 0.65 1.02 1.05 1.03 0.8 0.96 159 S159V 0.70 1.14 1.14 1.05 0.5 0.66 159 S159W 0.43 0.93 1.04 1.06 0.2 0.54 159 S159Y 0.37 1.07 1.11 1.27 0.5 0.90 160 G160A 0.51 0.83 0.96 0.81 0.6 0.63 160 G160C 0.85 0.75 1.06 0.83 0.9 0.86 160 G160D 1.17 0.71 1.28 0.88 1.0 0.90 160 G160E 1.05 0.85 1.31 0.92 1.0 0.92 160 G160K 0.79 0.75 0.79 0.88 0.4 0.89 160 G160L 0.36 0.92 1.00 1.00 0.5 0.52 160 G160M 0.41 0.70 0.86 0.87 0.4 0.46 160 G160N 0.92 1.05 1.21 0.93 0.9 1.00 160 G160P 0.51 0.82 1.15 0.69 0.7 0.63 160 G160Q 0.75 0.72 1.15 0.92 0.8 0.83 160 G160R 0.54 0.69 0.83 0.87 0.3 0.78 160 G160S 0.80 0.82 1.12 0.89 0.7 0.84 160 G160T 0.71 0.70 1.21 1.08 0.6 0.93 160 G160V 0.48 1.12 1.25 0.88 0.5 0.60 160 G160W 0.37 0.93 0.90 0.99 0.3 0.61 160 G160Y 0.46 0.90 1.11 1.06 0.4 0.61 161 S161A 1.08 1.15 1.21 0.95 0.8 1.00 161 S161C 1.31 0.93 1.12 0.82 1.2 1.04 161 S161E 1.35 1.12 1.21 1.00 1.2 0.92 161 S161F 0.58 0.96 1.18 1.02 0.9 1.17 161 S161G 1.37 1.13 1.14 0.96 1.1 0.93 161 S161I 1.01 1.18 1.10 0.94 0.9 0.86 161 S161K 0.97 0.88 1.00 1.02 0.9 1.04 161 S161L 1.12 1.25 0.96 0.87 1.0 0.96 161 S161M 1.07 1.08 1.03 0.99 1.0 0.95 161 S161P 1.30 1.26 1.19 1.07 1.0 1.04 161 S161Q 1.10 1.16 1.13 0.98 1.1 1.15 161 S161R 0.84 0.94 0.84 0.88 0.8 1.16 161 S161T 1.13 1.09 1.21 1.00 1.0 1.41 161 S161V 0.93 1.29 1.07 1.05 0.9 1.10 161 S161W 0.43 0.96 1.12 1.05 0.7 0.83 161 S161Y 0.70 1.05 1.05 0.95 0.8 0.99 162 S162A 0.75 1.09 1.00 0.96 1.0 0.92 162 S162C 1.24 0.94 0.95 0.89 1.1 0.93 162 S162E 1.41 1.16 0.93 0.89 1.1 0.99 162 S162F 0.45 0.94 0.96 0.82 0.9 0.77 162 S162G 0.76 1.16 0.94 0.91 1.0 1.03 162 S162H 1.29 0.95 0.71 1.02 1.0 1.02 162 S162I 0.53 1.06 0.84 0.89 1.0 0.98 162 S162K 1.38 1.05 0.81 0.94 1.0 1.09 162 S162L 0.66 1.25 0.55 0.91 1.0 0.84 162 S162M 0.73 1.09 0.64 1.03 0.9 1.00 162 S162N 1.39 0.89 0.87 1.00 1.1 1.09 162 S162P 0.56 1.06 0.87 0.89 0.7 0.66 162 S162Q 1.28 1.06 1.06 0.88 1.1 1.07 162 S162R 0.90 0.80 0.69 0.89 0.9 1.26 162 S162T 0.89 1.04 0.69 0.76 0.9 0.98 162 S162V 0.61 1.13 0.81 0.92 0.9 1.03 162 S162W 0.50 1.03 0.55 0.68 0.7 0.71 163 S163A 0.32 0.71 0.78 0.89 0.2 0.30 163 S163C 0.35 0.88 0.55 0.85 0.2 0.26 163 S163D 0.56 0.92 0.90 0.86 0.1 0.45 163 S163G 1.10 1.02 0.86 0.93 0.6 0.85 163 S163H 0.25 0.97 0.70 0.98 0.1 0.29 163 S163I 0.31 0.73 0.72 0.93 0.1 0.20 163 S163P 0.99 1.05 0.78 0.95 0.4 0.63 163 S163R 0.27 0.67 0.55 0.77 0.1 0.24 163 S163T 0.45 0.95 1.01 1.06 0.7 0.60 163 S163W 0.21 1.05 0.96 0.95 0.1 0.20 164 T164A 0.38 0.40 0.53 0.76 0.1 0.21 164 T164C 0.29 0.51 0.70 0.74 0.1 0.11 164 T164E 0.39 0.79 1.27 1.14 0.8 0.43 164 T164G 0.40 0.51 0.76 0.70 0.1 0.26 164 T164I 0.19 0.44 0.67 0.86 0.3 0.07 164 T164L 0.22 0.90 1.06 1.33 0.1 0.18 164 T164M 0.30 0.40 0.66 0.81 0.4 0.19 164 T164N 0.36 0.71 0.78 0.92 0.4 0.51 164 T164S 0.32 0.80 0.98 0.87 0.4 0.45 164 T164V 0.26 0.55 0.80 0.88 0.1 0.19 164 T164W 0.18 1.58 2.34 1.67 0.1 0.20 164 T164Y 0.20 1.10 1.76 1.62 0.1 0.19 165 V165C 0.22 0.53 0.65 0.92 0.4 0.23 165 V165I 0.37 0.89 1.17 1.15 1.1 0.87 165 V165L 0.28 0.62 0.66 1.12 0.8 0.54 165 V165M 0.30 0.61 0.84 1.10 0.7 0.53 165 V165P 0.46 0.87 0.80 0.84 0.8 0.70 165 V165T 0.19 1.50 1.95 1.86 0.1 0.21 166 G166A 0.27 0.47 0.77 0.97 1.1 0.26 166 G166C 0.86 0.61 0.78 0.79 1.1 0.33 166 G166F 1.09 0.54 0.46 0.82 1.3 0.17 166 G166H 1.04 0.80 0.77 0.78 1.2 0.41 166 G166K 0.82 0.32 0.33 0.58 0.9 0.43 166 G166L 1.36 0.41 0.48 0.61 1.2 0.20 166 G166M 1.13 0.56 0.59 0.66 1.1 0.40 166 G166N 1.08 0.90 0.94 1.10 1.1 0.47 166 G166P 0.37 0.79 0.83 0.88 0.1 0.19 166 G166Q 1.21 0.66 0.81 0.96 1.1 0.57 166 G166R 0.87 0.41 0.43 0.88 0.9 0.55 166 G166S 1.09 0.80 1.04 0.75 1.0 0.26 166 G166W 1.10 0.65 0.95 0.99 1.1 0.06 166 G166Y 0.99 0.69 0.45 0.92 1.0 0.19 167 Y167A 0.68 1.35 1.13 1.28 0.7 0.57 167 Y167C 0.42 1.20 1.06 1.31 0.6 0.30 167 Y167D 0.27 1.36 1.64 1.29 0.1 0.07 167 Y167E 0.37 1.46 1.71 1.31 0.5 0.08 167 Y167F 1.01 0.96 1.11 0.99 0.9 0.83 167 Y167H 0.33 0.93 1.06 1.15 0.5 0.47 167 Y167I 0.66 0.98 1.15 1.14 0.9 0.34 167 Y167L 0.23 1.16 1.53 1.29 0.1 0.17 167 Y167M 0.23 1.69 1.28 1.35 0.4 0.22 167 Y167S 0.30 1.37 1.27 1.32 0.2 0.30 167 Y167T 0.33 1.47 1.25 1.39 0.3 0.35 167 Y167V 0.60 0.96 1.06 1.07 0.8 0.44 167 Y167W 0.41 1.21 1.10 1.04 0.3 0.54 169 G169A 1.32 0.86 0.90 0.89 1.0 1.23 169 G169C 0.19 3.00 2.18 2.35 1.0 0.46 169 G169S 0.38 1.02 0.83 1.03 0.9 0.63 170 K170A 1.04 1.16 1.09 0.98 1.1 1.23 170 K170C 0.81 1.19 1.03 0.95 0.9 0.73 170 K170F 0.50 1.09 1.09 0.95 0.9 0.69 170 K170G 0.51 1.21 0.92 1.00 0.9 0.65 170 K170H 0.57 1.10 1.10 0.98 0.8 0.86 170 K170I 0.47 1.19 1.14 0.93 0.7 0.43 170 K170L 0.36 1.27 1.15 0.97 0.7 0.33 170 K170M 0.39 1.04 0.96 0.99 0.6 0.38 170 K170N 0.34 1.59 1.37 1.18 0.5 0.58 170 K170P 0.22 2.48 2.58 1.55 0.9 0.65 170 K170Q 0.51 1.32 1.22 1.05 0.8 0.63 170 K170R 1.13 1.12 1.08 1.05 1.1 1.14 170 K170S 0.51 1.30 1.13 0.90 0.9 0.75 170 K170T 0.29 1.48 1.50 1.06 0.5 0.48 170 K170V 0.62 1.13 1.17 1.08 0.8 0.78 170 K170W 0.30 1.08 1.13 0.97 0.8 0.48 170 K170Y 0.38 1.39 1.22 1.04 0.9 0.66 171 Y171C 0.17 12.33 8.58 1.82 0.8 0.12 171 Y171F 0.47 1.24 0.88 0.93 0.7 0.68 171 Y171L 0.18 4.11 3.35 2.44 0.3 0.25 171 Y171W 0.49 1.37 1.02 1.02 0.6 0.40 172 P172A 0.83 1.13 1.08 1.09 1.0 1.14 172 P172C 0.69 1.22 1.17 0.77 0.9 1.06 172 P172E 0.80 1.30 1.16 1.01 1.2 1.01 172 P172F 0.40 1.25 0.99 1.14 0.8 0.92 172 P172G 0.34 1.36 1.22 1.23 1.0 0.87 172 P172H 0.52 1.09 0.91 1.08 0.9 1.03 172 P172I 0.46 1.38 1.11 1.11 0.9 1.07 172 P172K 0.66 0.99 0.61 0.90 1.0 1.05 172 P172L 0.52 1.50 1.08 1.14 1.0 1.02 172 P172M 0.55 1.23 1.14 1.08 1.0 1.02 172 P172N 0.67 1.09 0.96 1.01 0.9 1.05 172 P172Q 0.75 1.17 1.02 0.90 1.0 1.19 172 P172R 0.52 0.84 0.51 0.80 1.0 0.99 172 P172S 0.64 1.17 1.02 1.20 1.0 1.06 172 P172T 0.58 1.27 1.04 1.15 0.8 1.24 172 P172V 0.54 1.37 1.18 1.24 0.8 1.15 172 P172Y 0.29 1.67 1.29 1.41 0.8 0.88 173 S173A 0.89 1.16 0.72 1.02 0.9 0.93 173 S173C 0.81 1.19 0.89 1.05 0.9 0.98 173 S173E 0.96 0.90 0.78 0.98 1.0 0.95 173 S173F 0.51 1.07 1.17 0.87 0.6 0.82 173 S173G 0.64 0.93 0.65 0.91 0.8 0.59 173 S173H 0.49 1.35 0.88 1.18 0.8 0.92 173 S173I 0.44 1.16 1.05 1.30 0.8 1.10 173 S173K 0.70 0.66 0.57 1.03 0.7 0.95 173 S173L 0.56 1.10 1.02 1.35 0.9 0.84 173 S173M 0.69 1.11 1.16 1.00 0.8 1.01 173 S173P 0.45 1.14 1.02 1.22 0.9 0.89 173 S173Q 0.67 1.28 0.84 1.21 0.9 1.03 173 S173R 0.45 0.98 0.65 1.14 0.6 0.93 173 S173T 0.82 1.08 0.81 1.15 1.0 1.00 173 S173V 0.79 1.09 0.79 1.10 1.0 1.09 173 S173W 0.33 1.89 1.29 1.50 0.6 0.90 173 S173Y 0.39 1.71 1.01 1.38 0.7 0.87 174 V174A 0.45 1.44 1.21 1.10 0.8 1.00 174 V174C 0.80 1.14 1.08 1.21 0.9 1.19 174 V174I 0.37 1.48 0.86 1.14 0.6 0.58 174 V174L 0.21 92.96 66.79 4.24 0.5 0.34 174 V174S 0.41 1.38 1.04 1.21 0.9 0.82 174 V174T 0.78 1.29 0.82 1.13 0.9 1.11 175 I175A 0.21 6.10 9.32 1.84 0.4 0.31 175 I175C 0.61 1.10 1.06 1.16 0.9 0.92 175 I175F 0.32 1.69 1.23 1.30 0.6 0.81 175 I175L 0.90 1.27 0.89 1.04 0.8 1.10 175 I175M 0.92 1.17 0.82 1.05 1.0 0.98 175 I175T 0.31 1.96 1.59 1.44 0.5 0.93 175 I175V 0.33 1.96 1.32 1.36 0.9 1.06 176 A176C 1.04 0.99 0.79 1.00 1.1 1.15 176 A176G 0.24 0.55 0.86 1.10 0.5 0.37 176 A176S 0.78 0.89 1.00 1.12 1.0 0.71 176 A176T 0.58 1.19 1.12 1.24 1.1 0.77 177 V177A 0.67 0.50 0.83 0.93 0.4 0.82 177 V177C 0.49 0.77 0.95 1.10 0.7 0.83 177 V177I 0.37 0.89 1.25 1.25 0.5 0.89 177 V177S 0.34 0.87 0.97 1.16 0.1 0.72 177 V177T 0.56 0.75 0.73 1.09 0.8 1.00 177 V177W 0.18 3.77 5.40 4.51 0.2 0.53 179 A179G 0.92 1.06 0.88 1.19 0.4 0.72 179 A179M 0.21 0.36 0.57 0.65 0.1 0.13 179 A179S 0.63 1.04 0.74 1.16 0.4 0.74 180 V180A 0.70 0.98 0.76 1.05 0.1 0.78 180 V180C 0.99 1.03 0.73 1.08 1.0 0.91 180 V180H 0.17 2.27 2.90 1.90 0.1 0.14 180 V180L 1.08 0.98 0.64 1.06 0.9 1.05 180 V180S 0.90 0.96 0.94 1.04 0.3 1.01 180 V180T 1.07 0.93 0.87 1.01 0.9 1.13 181 D181C 0.80 0.88 0.79 0.89 0.5 0.84 181 D181E 0.86 1.01 0.71 1.22 0.3 0.86 181 D181N 1.07 0.79 0.62 0.93 0.2 1.06 182 S182A 0.96 0.97 1.09 1.02 0.9 0.94 182 S182C 1.10 1.03 1.06 0.85 1.1 1.00 182 S182D 0.92 1.22 1.07 1.01 1.1 1.06 182 S182F 0.88 1.14 1.07 1.00 0.4 1.20 182 S182G 1.16 1.09 1.03 1.00 0.9 0.81 182 S182H 1.09 1.13 1.04 0.93 0.8 0.91 182 S182I 0.87 1.13 1.17 1.15 0.7 1.15 182 S182L 0.88 0.88 1.07 0.98 0.4 1.00 182 S182M 1.00 0.96 1.22 0.95 0.8 1.05 182 S182P 1.26 0.77 1.17 1.00 0.9 0.77 182 S182Q 0.94 1.28 1.04 0.98 1.0 1.08 182 S182T 0.95 0.82 1.19 0.92 0.8 0.98 182 S182V 0.79 1.02 1.31 1.07 0.8 1.19 182 S182W 0.32 1.48 1.36 1.36 0.3 1.04 182 S182Y 0.86 1.07 1.05 0.98 0.5 1.22 183 S183A 1.09 0.88 1.12 1.03 0.9 0.99 183 S183C 1.09 1.22 1.01 0.91 1.1 0.84 183 S183E 1.06 0.84 1.01 0.93 1.2 1.04 183 S183F 0.97 0.91 1.35 0.83 0.9 1.06 183 S183G 0.98 0.77 0.97 1.04 1.0 0.84 183 S183H 1.10 1.10 0.84 1.00 1.0 0.85 183 S183I 1.11 1.07 1.02 1.01 0.9 1.02 183 S183K 1.08 0.68 0.67 0.95 0.2 0.93 183 S183L 1.02 0.84 0.85 1.00 1.0 1.01 183 S183M 1.05 1.03 1.23 1.05 1.0 0.87 183 S183N 1.08 0.85 1.02 1.02 1.1 0.95 183 S183Q 0.99 0.66 1.23 0.98 1.1 0.95 183 S183R 1.06 0.67 0.70 0.95 0.1 0.93 183 S183T 0.92 1.20 1.25 1.02 1.0 1.12 183 S183V 0.90 1.20 1.10 0.93 1.0 1.11 183 S183W 0.71 1.03 1.00 1.06 0.7 1.26 183 S183Y 0.95 0.89 0.91 1.12 1.0 1.11 184 N184A 0.27 1.40 1.89 1.40 0.7 0.71 184 N184C 0.90 1.16 1.02 1.06 1.0 1.10 184 N184D 0.90 1.03 1.20 0.96 1.1 0.96 184 N184E 0.83 1.18 1.09 0.90 0.9 1.06 184 N184F 0.84 0.86 0.99 1.14 0.5 1.03 184 N184G 0.99 0.91 1.19 0.93 0.8 0.91 184 N184H 0.94 1.06 1.11 1.02 0.6 0.97 184 N184I 0.75 1.04 1.07 0.98 0.2 1.03 184 N184L 0.95 1.36 0.87 1.09 0.7 0.93 184 N184M 1.05 0.99 1.06 0.97 0.7 0.97 184 N184P 0.78 0.78 1.02 0.79 0.1 0.82 184 N184Q 0.82 0.78 1.10 1.10 0.6 1.05 184 N184S 0.88 1.02 0.97 1.06 0.7 1.04 184 N184T 0.80 1.16 1.14 0.90 0.4 1.19 184 N184V 0.72 1.30 1.07 1.02 0.3 1.02 184 N184W 0.80 0.92 1.28 0.99 0.4 1.26 184 N184Y 0.80 0.93 1.06 1.16 0.6 1.10 185 Q185A 1.01 0.84 1.15 1.06 0.9 1.08 185 Q185C 0.95 1.15 1.09 0.92 1.1 1.00 185 Q185D 0.29 2.02 1.65 1.42 0.6 0.56 185 Q185E 0.77 1.37 1.07 0.91 1.2 1.03 185 Q185F 0.84 1.05 1.09 0.94 0.6 1.14 185 Q185G 0.74 0.79 1.29 1.00 0.7 1.02 185 Q185H 1.00 0.88 0.91 1.02 0.9 1.09 185 Q185I 0.87 1.46 0.98 0.95 0.9 1.24 185 Q185K 0.98 0.68 0.73 0.85 0.7 0.97 185 Q185L 0.87 0.99 0.96 1.04 0.7 1.00 185 Q185M 0.93 0.91 1.09 1.05 1.0 1.01 185 Q185N 0.97 1.14 1.11 1.08 1.1 1.05 185 Q185R 0.91 0.75 0.80 0.99 0.4 1.07 185 Q185S 0.83 1.38 1.04 1.06 0.8 1.06 185 Q185T 0.82 1.36 1.28 1.13 1.0 1.17 185 Q185V 0.94 1.04 1.30 0.99 0.8 1.16 185 Q185W 0.81 0.85 0.85 0.87 0.1 1.14 185 Q185Y 0.74 0.95 1.05 1.26 0.7 1.28 186 R186A 0.38 1.03 1.51 1.09 0.7 0.45 186 R186C 0.36 1.91 1.61 1.05 0.6 0.47 186 R186E 0.21 23.12 23.90 1.79 0.1 0.11 186 R186F 0.33 1.32 1.44 0.88 0.2 0.29 186 R186G 0.31 2.21 1.88 1.19 0.2 0.60 186 R186H 0.50 1.13 1.34 1.17 0.7 0.73 186 R186I 0.38 1.34 2.12 1.26 0.9 0.80 186 R186K 0.62 0.95 1.19 1.00 0.6 0.92 186 R186L 0.54 1.58 1.44 1.20 0.9 0.89 186 R186N 0.25 2.46 3.74 1.52 0.3 0.43 186 R186P 0.24 2.96 2.29 0.95 0.1 0.19 186 R186Q 0.37 1.48 2.05 1.32 0.8 0.85 186 R186S 0.27 2.44 1.91 1.39 0.3 0.40 186 R186T 0.22 8.56 6.97 2.69 0.4 0.36 186 R186V 0.42 2.00 2.04 1.42 0.9 0.75 186 R186W 0.63 1.54 1.71 1.12 1.1 0.98 186 R186Y 0.38 1.50 1.98 1.37 0.8 0.71 187 A187C 0.77 0.75 1.06 0.84 0.2 0.31 187 A187D 0.93 1.51 0.99 1.03 0.4 0.17 187 A187E 0.72 1.41 1.49 1.00 0.2 0.34 187 A187F 0.73 1.02 1.07 0.93 0.1 0.43 187 A187G 0.90 1.04 1.12 0.93 0.6 1.05 187 A187N 0.74 1.11 1.39 1.03 0.5 1.22 187 A187P 1.08 1.15 1.12 0.92 0.7 0.69 187 A187S 0.68 1.14 1.13 1.06 0.4 0.94 187 A187W 0.93 0.95 0.99 1.07 0.7 0.41 187 A187Y 1.02 1.05 1.25 0.79 0.5 0.40 188 S188A 1.14 0.93 1.08 0.96 0.9 0.92 188 S188C 1.24 1.07 1.27 0.81 1.0 0.85 188 S188D 1.08 1.03 1.33 0.94 1.2 0.86 188 S188E 1.03 1.18 1.29 0.98 1.1 1.00 188 S188F 0.91 0.98 1.08 0.86 0.8 0.92 188 S188G 1.06 0.99 1.09 0.94 0.9 0.89 188 S188H 1.01 0.92 1.00 0.91 0.9 1.01 188 S188I 0.94 0.79 1.24 1.01 0.9 0.96 188 S188K 1.14 0.64 0.89 1.00 0.5 1.05 188 S188L 1.01 1.07 1.16 0.82 0.8 0.98 188 S188M 0.98 0.73 1.28 0.90 0.8 0.98 188 S188P 1.05 1.05 1.23 1.01 1.0 0.90 188 S188Q 0.97 1.01 1.17 1.00 0.9 1.03 188 S188R 0.48 0.91 1.28 1.13 0.5 1.00 188 S188T 0.82 0.95 1.37 1.01 0.9 1.08 188 S188V 0.84 0.97 1.25 0.96 0.8 1.15 188 S188W 0.80 0.63 1.04 0.70 0.8 0.81 188 S188Y 0.77 0.90 1.11 0.86 0.9 0.94 189 F189C 1.16 0.82 0.77 0.86 0.3 0.15 189 F189D 2.06 1.03 0.88 0.94 0.4 0.28 189 F189M 1.67 1.01 0.89 1.02 0.1 0.40 189 F189N 1.31 0.83 0.77 0.82 0.1 0.83 189 F189S 0.93 0.91 1.08 1.06 0.1 0.81 189 F189T 0.74 1.01 1.10 0.99 0.1 0.92 189 F189W 0.59 0.57 0.71 0.81 1.0 0.54 189 F189Y 0.66 0.62 0.86 0.96 0.5 0.53 190 S190A 0.35 1.19 1.27 0.80 0.1 0.57 190 S190C 0.62 0.82 1.11 0.69 0.6 0.68 190 S190G 0.27 1.50 2.17 1.30 0.1 0.56 190 S190N 0.23 1.60 2.04 1.06 0.1 0.12 190 S190T 0.31 1.03 1.36 1.15 0.3 0.49 191 Q191A 0.93 0.67 1.11 0.98 0.9 0.66 191 Q191C 0.44 0.72 0.91 0.96 0.3 0.32 191 Q191G 0.77 0.75 0.73 0.74 0.7 0.33 191 Q191N 0.72 0.70 1.34 1.14 0.1 0.56 191 Q191T 0.32 1.03 0.92 0.82 0.1 0.10 191 Q191V 0.33 0.98 0.62 0.74 0.1 0.09 192 Y192A 0.86 0.94 1.08 0.97 0.8 1.08 192 Y192D 0.24 1.91 2.19 1.17 0.1 0.11 192 Y192F 0.51 0.70 0.98 0.87 0.4 0.55 192 Y192G 0.43 0.66 0.98 0.99 0.2 0.47 192 Y192H 0.45 0.85 0.66 0.82 0.2 0.49 192 Y192M 0.41 0.90 0.93 0.84 0.1 0.39 192 Y192N 0.33 1.16 1.47 1.01 0.1 0.66 192 Y192P 0.34 0.88 0.38 0.60 0.1 0.13 192 Y192Q 0.36 2.14 1.27 1.17 0.2 0.56 192 Y192S 0.63 0.82 1.15 0.93 0.7 0.88 192 Y192T 0.72 0.73 1.08 0.98 0.9 0.93 194 P194A 0.69 1.09 0.94 0.95 0.8 1.16 194 P194C 0.75 1.19 1.18 1.19 1.0 1.41 194 P194E 0.70 1.52 1.09 1.03 1.0 1.25 194 P194G 0.48 1.23 0.92 1.12 0.7 0.81 194 P194H 0.76 1.13 1.00 1.15 1.0 1.03 194 P194I 0.48 1.63 1.09 1.21 0.9 1.12 194 P194K 0.72 0.79 0.90 0.90 0.6 0.98 194 P194L 0.58 1.58 0.87 1.29 0.9 1.09 194 P194M 0.60 1.36 1.09 1.06 0.8 1.47 194 P194N 0.52 1.82 1.00 1.23 0.1 1.69 194 P194Q 0.60 1.24 1.02 1.16 0.8 1.09 194 P194S 0.69 1.19 0.94 1.13 0.8 1.10 194 P194T 0.58 1.32 1.37 1.10 0.9 1.21 194 P194V 0.48 1.67 1.08 1.18 0.8 1.36 194 P194W 0.57 1.27 1.17 1.10 0.9 1.16 195 E195A 0.26 0.78 0.71 0.64 0.1 0.26 195 E195C 0.25 1.37 0.92 0.57 0.4 0.22 195 E195D 0.34 1.09 0.84 0.86 0.7 0.38 195 E195G 0.71 0.95 0.44 0.77 0.3 0.52 195 E195H 0.26 0.67 0.38 0.48 0.1 0.08 195 E195K 0.22 3.69 2.57 2.17 0.3 0.47 195 E195Q 0.30 1.29 0.69 1.02 0.2 0.69 195 E195W 0.22 4.29 1.26 1.32 0.1 0.10 196 L196I 0.38 1.68 1.15 1.17 0.8 1.03 196 L196M 0.37 1.52 1.04 1.06 0.2 0.72 196 L196T 0.24 3.86 2.91 2.68 1.0 0.69 196 L196V 0.34 1.95 1.28 1.45 0.7 0.79 197 D197A 0.45 0.74 1.09 1.05 0.5 0.66 197 D197C 0.38 1.02 1.11 0.97 0.3 0.55 197 D197G 0.37 1.06 1.07 1.18 0.3 0.60 197 D197M 0.18 1.52 0.68 1.10 0.1 0.09 197 D197N 0.86 0.93 1.16 0.88 0.5 0.85 197 D197S 0.28 0.18 0.28 0.35 0.9 0.11 197 D197T 0.53 0.94 1.20 1.14 0.5 0.88 198 V198A 0.58 0.88 0.86 1.11 0.2 0.96 198 V198C 0.84 0.78 1.11 1.00 0.8 0.94 198 V198D 0.20 1.23 1.82 1.45 1.1 0.34 198 V198F 0.76 0.78 0.72 1.00 0.9 0.76 198 V198H 0.20 0.57 1.01 0.96 0.2 0.18 198 V198I 0.83 0.41 0.94 0.98 1.0 0.87 198 V198L 0.90 0.67 0.73 0.94 1.0 1.13 198 V198M 0.75 0.78 1.03 1.08 0.8 0.96 198 V198T 0.42 0.99 1.05 1.06 0.2 1.05 198 V198Y 0.53 0.67 1.19 1.12 0.8 1.00 199 M199A 0.49 1.04 0.94 1.10 0.1 0.79 199 M199C 0.64 0.88 0.85 0.80 0.7 0.66 199 M199F 0.17 28.65 28.81 2.58 0.1 0.23 199 M199G 0.18 1.09 0.55 0.93 0.1 0.12 199 M199Q 0.23 2.11 1.65 1.69 0.8 0.63 199 M199S 0.54 1.12 0.88 1.00 0.3 0.93 199 M199T 0.53 1.22 1.06 1.02 0.3 0.87 199 M199V 0.66 1.14 0.97 0.96 0.9 1.05 200 A200C 0.70 1.32 0.86 1.16 0.6 1.17 200 A200G 0.83 1.19 1.05 1.08 0.6 1.08 200 A200N 0.47 1.33 1.20 1.17 0.7 1.28 200 A200S 0.72 1.23 0.80 1.07 0.5 0.91 200 A200T 0.35 1.73 0.95 1.35 0.2 0.71 201 P201A 0.65 0.61 0.87 1.08 0.9 0.79 201 P201C 0.47 1.07 0.95 1.30 0.2 1.06 201 P201G 0.54 0.42 1.08 1.21 0.6 0.91 201 P201H 0.40 0.65 1.21 1.15 0.1 0.90 201 P201I 0.18 1.05 0.64 1.28 0.1 0.12 201 P201N 0.41 1.05 1.26 1.38 0.1 0.75 201 P201S 0.43 0.66 1.21 1.35 0.1 1.06 201 P201Y 0.58 0.73 0.91 1.11 0.7 1.17 203 V203A 0.51 1.07 1.26 1.24 0.3 1.48 203 V203C 0.93 1.10 1.10 0.83 1.0 0.66 203 V203D 0.54 1.12 1.62 1.23 1.1 1.09 203 V203E 0.57 0.88 1.05 1.13 1.1 0.88 203 V203G 0.17 8.72 7.71 4.86 0.1 0.33 203 V203H 0.59 0.87 0.81 0.89 0.1 0.30 203 V203I 0.81 0.63 1.05 0.93 0.8 0.77 203 V203M 0.77 0.98 1.14 1.00 0.6 0.99 203 V203N 0.47 1.05 1.38 1.22 0.1 0.99 203 V203Q 0.62 0.90 1.18 1.13 0.5 1.19 203 V203S 0.55 0.93 1.10 1.04 0.2 1.07 203 V203T 0.65 0.90 1.31 1.07 0.6 1.01 203 V203Y 0.43 0.94 1.21 1.05 0.1 0.97 204 S204A 0.97 0.86 1.00 0.81 1.2 1.06 204 S204C 0.90 1.00 1.05 0.89 1.4 0.85 204 S204F 0.86 0.39 0.60 0.82 0.7 1.06 204 S204G 0.88 1.01 1.19 0.75 1.1 1.50 204 S204H 0.68 0.72 0.81 0.95 1.0 1.21 204 S204I 0.66 0.79 0.99 0.83 0.7 0.91 204 S204K 0.90 0.74 0.64 0.87 0.1 0.93 204 S204L 0.77 0.85 0.82 0.93 0.9 0.90 204 S204M 0.90 0.75 1.10 0.95 0.8 0.90 204 S204Q 0.87 0.84 1.06 0.94 1.3 0.96 204 S204T 0.92 0.78 0.86 0.80 0.9 1.09 204 S204V 0.82 0.71 0.79 0.85 0.7 1.20 204 S204W 0.74 0.39 0.67 0.79 0.6 0.97 204 S204Y 0.75 0.52 1.04 0.87 0.7 1.03 205 I205T 0.77 1.60 1.20 1.11 0.8 1.29 205 I205V 0.95 1.25 1.08 1.11 1.3 1.03 206 Q206A 1.09 0.84 1.24 1.05 0.7 0.72 206 Q206C 1.10 1.13 1.03 1.12 1.4 0.94 206 Q206D 1.02 1.23 1.04 1.01 1.3 0.84 206 Q206E 1.01 1.26 1.14 1.16 1.4 0.97 206 Q206H 1.06 1.00 0.97 1.11 1.0 0.92 206 Q206I 1.12 1.00 0.99 1.04 0.5 0.87 206 Q206K 1.11 0.84 0.75 1.13 0.1 0.86 206 Q206L 1.03 0.89 0.93 0.94 0.7 1.02 206 Q206M 0.77 1.09 0.93 1.06 0.8 0.95 206 Q206N 1.03 1.07 1.08 1.06 1.1 0.91 206 Q206P 0.94 1.01 1.00 1.02 0.9 0.86 206 Q206S 0.92 1.21 0.98 1.00 0.9 0.97 206 Q206T 0.99 0.91 0.95 1.10 0.8 0.92 206 Q206V 1.01 1.04 1.19 1.11 0.6 1.07 206 Q206Y 1.04 0.96 0.96 1.18 0.9 0.93 208 T208A 0.89 1.28 1.15 1.12 0.1 1.02 208 T208C 0.82 1.48 1.13 1.24 0.8 1.14 208 T208D 0.27 0.78 0.73 0.35 0.2 0.20 208 T208M 0.22 5.66 6.03 1.79 0.4 0.37 208 T208S 0.81 1.20 1.16 1.01 0.2 1.24 209 L209A 1.06 0.51 0.27 0.77 0.6 0.43 209 L209C 0.82 1.41 1.04 1.05 0.9 1.53 209 L209E 0.98 0.69 0.36 0.76 0.8 0.71 209 L209F 0.72 1.26 1.05 1.15 0.2 2.25 209 L209G 1.00 0.51 0.33 0.60 0.3 0.26 209 L209H 0.64 0.45 0.25 0.62 0.6 0.14 209 L209K 0.88 0.81 0.69 1.05 0.3 1.20 209 L209M 0.71 1.26 1.09 1.16 0.8 1.83 209 L209Q 0.84 0.97 0.44 0.89 0.7 0.99 209 L209S 0.99 0.52 0.27 0.63 0.5 0.36 209 L209T 0.81 0.77 0.35 0.82 0.5 0.88 209 L209V 0.83 1.20 1.01 1.00 0.6 0.82 209 L209W 0.78 1.43 0.96 1.11 0.3 1.27 209 L209Y 0.62 0.95 0.64 1.01 0.1 1.47 210 P210A 0.66 1.12 0.81 0.89 0.3 0.93 210 P210C 0.42 1.52 0.90 0.96 0.2 0.75 210 P210D 0.32 1.40 0.78 1.18 0.1 0.26 210 P210E 0.37 1.67 1.08 1.31 0.4 0.69 210 P210F 0.21 10.28 3.47 2.00 0.1 0.11 210 P210S 0.58 1.35 1.10 1.15 0.4 1.25 210 P210T 0.55 1.15 1.10 1.34 0.3 1.10 210 P210V 0.49 1.36 1.24 1.13 0.2 0.75 211 G211A 0.90 1.54 1.09 1.04 1.0 0.92 211 G211C 1.13 0.68 1.18 0.94 1.1 0.86 211 G211D 0.95 1.52 1.15 0.99 1.4 0.95 211 G211E 0.92 1.31 1.08 1.10 1.3 0.90 211 G211F 0.85 1.21 1.09 1.15 0.6 1.08 211 G211K 0.90 1.05 0.90 0.95 0.4 1.03 211 G211L 0.67 1.22 1.18 1.12 0.7 0.86 211 G211M 0.88 1.22 1.21 0.99 0.9 0.96 211 G211N 0.92 1.29 1.12 1.00 1.0 0.99 211 G211P 0.86 1.32 1.66 1.01 0.6 0.99 211 G211Q 0.77 1.26 1.01 1.18 1.0 1.07 211 G211R 0.76 0.67 0.81 0.96 0.2 0.92 211 G211S 0.95 1.25 1.18 1.01 0.9 1.01 211 G211T 0.78 1.37 1.35 1.15 0.7 1.07 211 G211V 0.76 1.33 1.20 0.92 0.5 0.93 211 G211W 0.80 1.33 1.08 1.18 0.2 1.04 211 G211Y 0.86 1.01 1.27 1.16 0.8 1.04 212 N212A 1.18 0.98 1.29 0.99 0.8 0.67 212 N212C 1.06 1.04 1.20 0.92 0.9 1.13 212 N212E 0.97 1.44 1.12 0.93 1.2 0.75 212 N212F 1.08 0.91 1.01 0.95 0.5 0.75 212 N212G 0.80 1.14 1.32 0.98 0.9 0.92 212 N212H 0.95 1.22 1.11 0.94 0.6 1.21 212 N212I 0.49 0.41 0.41 0.24 0.5 0.20 212 N212K 0.79 0.82 0.75 0.99 0.1 0.85 212 N212L 0.83 0.63 0.69 0.76 0.2 0.75 212 N212M 1.06 1.08 1.04 1.09 0.5 0.87 212 N212P 0.99 0.96 0.85 1.00 0.3 0.78 212 N212Q 0.95 0.97 0.80 0.89 0.9 0.98 212 N212R 0.83 0.74 0.79 1.06 0.2 0.83 212 N212S 1.09 1.12 0.96 1.03 0.8 0.77 212 N212T 0.23 6.10 4.36 2.96 0.6 1.31 212 N212V 0.77 0.97 0.99 1.08 0.6 0.83 212 N212Y 0.93 1.05 0.85 0.96 0.4 0.98 213 K213A 1.05 1.23 1.22 0.95 1.4 0.91 213 K213C 0.96 1.03 1.03 0.86 1.4 0.99 213 K213D 1.01 1.13 1.20 0.89 1.4 0.86 213 K213E 0.96 0.99 1.09 0.89 1.5 0.84 213 K213F 0.92 1.20 1.26 0.98 1.1 0.93 213 K213H 1.01 1.29 1.07 0.97 1.3 1.09 213 K213I 1.02 1.01 1.14 0.94 1.2 0.96 213 K213L 1.03 1.13 1.17 1.03 1.3 1.17 213 K213M 1.06 1.13 1.17 1.04 1.5 1.03 213 K213N 1.02 1.26 1.17 1.00 1.7 0.95 213 K213Q 1.04 1.36 1.01 0.97 1.5 1.04 213 K213R 0.78 1.24 1.15 0.83 1.2 0.98 213 K213S 0.82 1.17 1.07 0.96 1.5 0.85 213 K213T 0.91 1.35 1.21 0.85 1.5 0.94 213 K213V 0.85 1.16 1.16 1.06 1.1 0.99 213 K213W 0.80 1.11 1.10 0.98 0.9 1.13 213 K213Y 0.85 1.15 1.01 0.97 1.3 0.96 214 Y214A 0.17 2.41 1.57 0.71 0.2 0.07 214 Y214D 0.18 3.22 3.18 1.71 0.2 0.12 214 Y214N 0.19 1.65 1.59 1.29 0.7 0.18 214 Y214S 0.18 2.22 1.06 1.50 0.2 0.10 215 G215A 0.99 1.16 0.99 0.98 0.6 0.58 215 G215C 1.00 1.03 1.06 0.82 0.8 0.70 215 G215D 0.89 1.33 1.10 1.06 1.0 0.70 215 G215E 1.04 1.22 1.16 0.84 1.0 0.75 215 G215H 0.64 1.16 0.76 1.05 0.1 0.72 215 G215M 0.72 1.23 1.00 0.82 0.1 0.59 215 G215Q 0.80 1.37 0.96 0.97 0.1 0.67 215 G215S 0.84 1.12 0.94 0.93 0.1 0.72 215 G215V 0.36 1.52 0.90 1.15 0.1 0.51 215 G215W 0.48 1.00 0.88 0.91 0.1 0.71 216 A216C 0.97 1.21 1.11 0.92 1.2 0.89 216 A216D 0.76 1.22 1.28 1.19 1.2 0.95 216 A216E 1.20 1.36 0.92 1.03 1.4 0.75 216 A216F 1.22 1.20 1.21 0.87 1.2 0.91 216 A216G 1.00 0.99 0.78 0.88 0.8 0.90 216 A216H 1.03 0.86 1.01 0.93 0.9 0.79 216 A216I 1.17 0.92 0.94 1.01 1.0 0.81 216 A216K 0.94 0.78 0.98 0.87 1.0 0.55 216 A216L 0.96 0.90 0.78 0.83 0.9 1.05 216 A216M 0.82 0.85 1.07 0.90 1.1 0.82 216 A216N 1.03 0.97 1.11 1.07 1.1 0.72 216 A216P 0.90 1.09 0.94 1.11 1.2 1.00 216 A216Q 1.03 0.96 1.14 1.09 0.9 0.94 216 A216R 1.12 0.54 0.62 0.92 0.1 0.90 216 A216S 0.73 1.00 1.09 1.22 0.9 1.03 216 A216V 0.92 1.13 0.93 0.94 0.9 1.15 216 A216W 0.96 0.55 0.86 0.77 0.9 0.73 216 A216Y 0.81 0.76 0.90 0.96 1.1 0.88 217 Y217C 1.03 0.98 0.86 0.95 1.6 1.34 217 Y217D 1.01 1.13 1.07 1.21 1.1 0.34 217 Y217E 1.00 1.40 0.99 1.18 1.3 0.54 217 Y217F 1.04 0.99 1.03 0.97 1.0 1.35 217 Y217G 0.85 0.81 0.72 0.95 1.0 0.97 217 Y217H 0.96 0.97 0.90 1.15 1.1 0.76 217 Y217I 0.84 1.16 1.24 1.14 0.7 1.53 217 Y217K 1.02 0.80 0.58 0.97 1.0 1.06 217 Y217L 0.98 1.34 0.97 1.07 1.4 3.46 217 Y217M 0.93 1.31 1.22 1.07 1.5 1.80 217 Y217N 0.78 0.94 0.65 0.91 1.0 1.21 217 Y217P 0.28 0.54 0.18 0.57 0.1 0.18 217 Y217Q 0.92 1.19 1.29 1.11 1.2 1.05 217 Y217R 1.00 0.80 0.54 1.01 0.9 0.87 217 Y217S 0.83 1.11 0.95 1.01 1.0 1.63 217 Y217T 0.80 1.03 0.63 1.10 0.8 1.15 217 Y217V 0.75 1.10 0.98 1.22 0.7 1.03 217 Y217W 0.80 0.76 0.68 0.79 1.0 0.71 218 N218A 0.99 0.94 0.92 0.97 0.7 1.13 218 N218C 1.05 1.06 0.86 0.83 1.1 0.76 218 N218E 0.90 1.03 1.09 0.85 1.1 0.59 218 N218F 0.77 0.62 0.55 0.78 0.2 0.97 218 N218G 0.88 1.06 1.07 1.01 0.5 1.23 218 N218H 0.94 1.02 0.93 0.91 0.9 0.61 218 N218I 0.52 0.45 0.43 0.57 0.1 0.36 218 N218M 0.76 0.95 0.74 0.75 0.4 0.94 218 N218P 0.29 1.56 0.82 1.19 0.2 0.60 218 N218S 1.00 1.00 0.99 1.07 1.2 1.07 218 N218T 0.93 0.62 0.73 0.73 0.9 0.58 218 N218V 0.48 0.51 0.64 0.50 0.2 0.77 218 N218W 0.70 0.65 0.59 0.65 0.3 0.68 218 N218Y 0.70 0.62 0.75 0.70 0.2 1.08 219 G219C 0.53 0.83 0.71 0.65 1.0 0.60 219 G219L 0.54 0.68 0.70 0.70 0.2 0.89 219 G219T 0.22 0.28 0.34 0.08 0.8 0.58 220 T220S 0.68 1.16 1.13 0.97 0.6 0.49 222 M222A 1.49 0.94 0.68 0.92 1.0 0.48 222 M222C 1.15 0.66 0.55 0.80 1.6 1.32 222 M222F 0.86 0.62 0.73 1.00 1.4 0.06 222 M222H 1.07 0.52 0.56 0.78 2.0 0.06 222 M222L 0.98 0.48 0.60 0.76 0.6 0.13 222 M222N 1.14 0.76 0.74 0.93 0.9 0.27 222 M222P 1.22 0.47 0.24 0.54 0.3 0.14 222 M222Q 0.78 0.97 0.87 1.19 1.4 0.12 222 M222S 1.15 0.77 0.62 0.87 1.0 0.95 222 M222T 1.12 0.64 0.46 0.72 1.0 0.34 222 M222V 1.20 0.69 0.50 0.80 0.9 0.12 222 M222W 1.89 0.36 0.21 0.74 0.7 0.09 223 A223G 0.62 1.00 0.60 0.86 0.2 0.66 223 A223S 1.05 0.95 1.00 0.91 0.9 0.72 223 A223T 0.23 1.22 0.73 0.91 0.2 0.17 224 S224A 1.14 1.24 1.14 1.15 0.9 1.16 224 S224C 1.34 1.23 1.23 1.22 1.1 0.65 224 S224G 0.90 1.23 1.15 1.13 0.3 0.63 224 S224N 0.35 1.77 1.55 1.26 0.6 0.24 224 S224T 0.66 1.16 1.22 1.07 0.9 0.37 224 S224V 0.97 0.89 0.90 1.05 0.9 0.06 225 P225S 1.13 0.37 0.40 0.55 0.9 0.07 227 V227A 1.03 0.99 1.26 0.83 1.0 0.81 227 V227C 0.95 1.01 1.29 1.01 0.9 0.81 227 V227F 0.30 0.87 1.35 1.00 0.5 0.74 227 V227G 0.32 1.55 1.43 1.06 0.9 0.69 227 V227I 0.97 1.12 1.06 0.82 0.7 0.95 227 V227L 0.50 1.36 1.30 1.04 0.4 0.92 227 V227M 0.36 0.76 1.18 0.87 0.7 0.75 227 V227S 0.16 14.70 19.48 4.22 0.5 0.53 227 V227T 0.63 1.04 1.44 1.01 0.7 0.87 228 A228G 0.38 1.14 1.11 1.31 1.0 0.66 228 A228I 0.23 1.27 0.90 1.50 0.2 0.23 228 A228M 0.22 0.86 0.93 1.15 0.4 0.20 228 A228S 0.88 0.86 1.10 1.17 1.1 0.80 228 A228T 0.78 1.04 1.04 1.07 1.0 0.68 228 A228V 0.37 1.18 1.37 1.39 0.9 0.51 229 G229A 1.20 0.82 1.12 0.99 0.8 0.99 229 G229S 0.76 0.75 0.96 1.03 0.6 1.03 230 A230C 1.06 0.88 1.21 1.12 0.8 1.06 230 A230E 0.77 0.74 1.09 1.06 0.6 0.75 230 A230F 0.50 0.52 1.30 1.06 1.1 0.94 230 A230G 0.99 0.86 1.16 0.95 1.0 0.98 230 A230H 0.16 10.35 16.17 3.82 0.1 0.38 230 A230N 0.19 1.80 2.19 1.72 0.6 0.58 230 A230Q 0.39 0.81 1.14 1.03 0.3 0.86 230 A230S 1.00 0.86 1.00 1.00 0.9 1.04 230 A230T 0.89 0.94 0.94 1.01 0.7 1.14 230 A230V 0.56 0.85 0.95 1.08 0.2 1.17 231 A231C 0.84 0.99 1.15 1.09 0.8 0.79 231 A231F 0.33 1.16 1.34 1.33 0.5 0.57 231 A231G 0.42 1.10 1.04 1.35 1.1 0.86 231 A231I 0.86 1.08 1.16 1.12 0.8 0.71 231 A231L 0.45 1.07 1.27 1.32 0.7 0.83 231 A231M 0.41 1.15 1.26 1.30 0.7 0.73 231 A231S 0.55 0.96 1.28 1.14 1.0 1.03 231 A231T 0.57 1.22 1.31 1.09 0.8 0.98 231 A231V 0.71 1.07 1.04 1.12 0.8 0.99 231 A231W 0.18 4.36 5.85 4.42 0.3 0.16 231 A231Y 0.25 1.52 2.14 1.63 0.2 0.44 232 A232C 0.92 1.09 1.13 1.00 0.9 0.99 232 A232E 0.28 0.25 0.21 0.37 1.0 0.14 232 A232L 0.37 1.15 1.29 1.42 1.1 0.87 232 A232M 0.66 1.02 1.04 0.98 1.0 0.91 232 A232N 0.20 1.64 2.16 1.52 1.1 0.44 232 A232S 0.81 0.96 1.27 0.93 0.9 0.94 232 A232T 0.73 0.97 1.02 1.03 1.0 1.04 232 A232V 0.77 1.00 1.35 0.99 1.0 1.09 233 L233D 0.71 0.89 0.91 0.92 1.1 0.71 233 L233I 0.85 0.89 1.11 1.03 1.0 0.90 233 L233M 0.67 0.92 0.99 1.01 0.9 0.94 233 L233S 0.61 1.05 1.16 0.96 0.9 0.78 233 L233T 0.78 0.95 1.25 0.90 1.0 0.89 233 L233V 0.94 1.15 1.09 0.89 1.1 0.91 234 I234A 1.16 0.86 0.96 0.88 0.8 1.12 234 I234C 1.21 1.02 0.92 0.96 1.1 0.88 234 I234D 0.21 0.70 1.52 0.91 0.6 0.44 234 I234E 0.88 1.05 1.01 0.86 0.8 1.01 234 I234F 0.72 1.03 1.02 0.72 0.1 1.02 234 I234G 0.33 0.93 0.96 1.15 0.7 0.86 234 I234H 0.37 0.98 0.98 0.97 0.3 0.94 234 I234K 0.30 0.89 0.92 1.00 0.1 0.84 234 I234L 1.22 0.82 0.84 1.08 1.1 1.07 234 I234M 1.27 1.02 0.91 0.98 1.0 1.18 234 I234N 0.42 1.08 0.98 1.03 0.9 0.91 234 I234Q 0.87 0.72 0.94 0.93 0.9 0.96 234 I234S 0.81 0.92 0.93 0.93 0.9 0.98 234 I234T 1.14 0.87 0.92 1.02 1.1 0.99 234 I234V 1.20 1.02 1.19 0.93 1.1 1.14 234 I234W 0.17 4.77 6.83 2.41 0.1 0.19 235 L235A 0.67 1.05 0.95 1.05 1.0 1.15 235 L235C 1.08 0.96 1.24 1.03 0.9 1.07 235 L235D 0.20 0.19 1.17 0.45 1.1 0.14 235 L235E 0.42 0.81 1.03 0.94 1.1 0.25 235 L235F 1.25 1.08 1.01 0.94 1.0 0.80 235 L235G 0.27 1.09 0.76 1.11 1.1 0.62 235 L235I 1.31 0.92 0.83 1.10 1.1 0.94 235 L235K 1.32 0.86 1.21 0.96 1.1 0.85 235 L235M 1.34 0.99 0.99 1.03 1.1 0.89 235 L235N 0.25 1.32 1.54 1.19 1.2 0.69 235 L235Q 1.01 0.92 0.84 1.03 1.1 1.24 235 L235R 1.29 0.79 0.86 0.95 1.0 0.90 235 L235S 0.69 1.05 0.86 0.76 1.0 1.00 235 L235T 0.65 1.10 0.80 0.86 1.1 1.07 235 L235V 1.17 0.92 1.07 0.83 1.1 1.24 235 L235W 1.09 0.98 0.63 1.13 1.1 0.94 235 L235Y 0.99 0.99 0.98 1.04 1.1 1.02 236 S236A 1.21 1.02 1.06 0.94 0.9 1.03 236 S236C 1.28 0.89 0.95 0.96 1.0 0.90 236 S236D 1.22 1.02 0.95 0.98 1.2 1.07 236 S236E 1.26 0.90 0.88 1.09 1.2 1.55 236 S236G 1.20 1.06 1.09 0.97 0.9 0.99 236 S236H 1.12 0.84 0.87 0.92 1.2 1.07 236 S236K 0.31 0.96 0.80 1.18 0.7 0.55 236 S236L 0.19 0.42 0.92 0.66 0.8 0.13 236 S236N 1.24 1.03 1.18 0.86 0.6 1.13 236 S236Q 1.18 0.85 0.69 0.95 1.1 1.00 236 S236R 0.34 0.96 0.72 1.13 0.7 0.60 236 S236T 0.59 0.99 0.97 1.04 0.8 1.16 236 S236V 0.91 0.97 0.86 1.06 0.9 1.21 236 S236W 0.18 2.11 3.43 2.28 0.8 0.50 236 S236Y 0.48 1.10 0.66 0.91 0.8 1.09 237 K237A 1.13 1.11 1.31 0.81 1.0 1.03 237 K237C 0.19 1.21 1.50 0.91 1.1 0.33 237 K237E 1.03 0.86 0.84 0.85 1.0 1.22 237 K237F 1.05 0.80 0.99 0.92 1.0 1.21 237 K237G 1.05 0.90 1.08 1.06 1.0 0.94 237 K237H 1.05 0.91 0.97 0.93 1.1 0.88 237 K237I 1.02 1.03 0.69 0.70 1.0 1.05 237 K237L 1.04 0.96 0.89 1.10 1.0 1.12 237 K237M 1.17 0.89 1.09 0.86 0.9 1.20 237 K237N 1.09 1.00 0.99 0.94 1.1 0.93 237 K237P 0.19 0.50 0.92 0.59 1.1 0.15 237 K237Q 1.12 0.74 0.87 0.84 1.1 1.01 237 K237R 1.13 0.82 0.95 1.02 1.0 1.08 237 K237S 1.17 0.97 1.07 0.86 1.0 1.24 237 K237T 1.07 0.81 0.75 0.82 1.0 0.94 237 K237V 1.08 0.85 1.09 1.10 0.9 1.09 237 K237W 0.81 0.96 1.08 0.95 0.9 0.87 237 K237Y 1.00 1.10 0.98 1.08 0.9 1.10 238 H238A 0.28 1.34 1.44 1.12 1.1 0.46 238 H238C 0.62 1.07 1.09 0.99 1.1 0.97 238 H238D 0.35 0.93 1.18 1.19 1.1 0.78 238 H238E 0.61 0.91 1.00 1.00 1.1 1.08 238 H238F 0.74 0.69 1.05 0.95 1.1 1.09 238 H238G 0.22 5.21 5.98 2.44 1.0 0.44 238 H238I 0.22 7.74 7.02 3.64 1.1 0.52 238 H238K 0.87 0.82 1.07 0.89 1.0 1.24 238 H238M 0.58 1.00 1.15 0.89 1.0 0.93 238 H238R 0.79 0.96 0.76 1.04 0.9 1.17 238 H238S 0.55 1.29 1.03 0.82 1.0 0.99 238 H238W 0.41 1.14 0.92 1.16 1.1 1.10 239 P239A 0.57 0.98 0.94 0.88 1.0 0.86 239 P239C 0.78 0.96 0.85 0.83 1.0 1.03 239 P239D 0.89 1.00 0.81 0.98 1.1 0.87 239 P239E 0.80 1.16 0.81 0.97 1.1 0.96 239 P239F 0.66 1.15 0.67 1.03 1.0 1.02 239 P239G 0.76 0.71 0.48 0.95 0.2 0.79 239 P239H 0.89 1.41 1.02 1.12 1.1 1.09 239 P239L 0.65 1.04 0.90 0.95 1.1 1.09 239 P239M 0.79 1.12 0.70 0.98 1.1 0.89 239 P239N 0.82 1.08 0.83 1.01 1.2 0.94 239 P239Q 0.91 1.14 0.80 1.10 1.2 0.97 239 P239R 0.92 1.21 0.67 1.27 1.0 1.04 239 P239S 0.87 1.31 0.96 0.99 1.1 1.33 239 P239T 0.80 0.97 1.07 1.11 1.2 1.03 239 P239V 0.71 1.10 1.22 1.06 1.2 1.32 239 P239W 0.65 1.06 0.75 1.11 1.0 1.28 239 P239Y 0.76 0.90 0.94 1.20 1.2 1.22 240 N240A 0.80 0.96 0.99 0.96 1.0 0.91 240 N240C 1.06 1.04 0.83 0.89 1.1 0.95 240 N240D 1.05 1.07 0.88 1.03 1.2 0.93 240 N240E 1.03 1.27 0.83 1.00 1.2 1.05 240 N240F 1.02 0.94 0.84 0.93 1.1 0.92 240 N240G 1.03 1.21 0.87 0.90 1.0 1.01 240 N240K 1.09 1.04 1.04 0.99 1.1 1.02 240 N240L 0.78 1.27 0.86 1.08 1.0 1.05 240 N240M 0.94 1.03 0.76 0.92 1.0 0.94 240 N240P 0.39 0.75 0.72 0.89 0.9 0.54 240 N240Q 0.91 1.09 0.88 1.11 1.1 1.04 240 N240R 0.75 0.85 0.59 1.14 1.0 0.97 240 N240S 1.00 1.19 1.04 1.11 1.1 0.95 240 N240T 0.90 1.02 0.77 1.14 1.1 1.02 240 N240V 0.90 1.06 0.92 1.06 1.0 1.10 240 N240W 1.05 1.05 0.66 1.01 1.0 1.00 240 N240Y 0.92 1.01 0.80 1.22 1.0 1.43 241 W241A 0.84 0.94 0.65 1.02 1.1 0.86 241 W241C 0.63 0.96 0.72 0.98 1.1 1.09 241 W241D 0.44 1.06 1.03 1.05 1.2 0.89 241 W241E 0.34 1.05 0.81 1.06 1.1 0.63 241 W241F 0.81 0.94 0.86 0.75 1.0 0.87 241 W241G 0.31 1.35 1.05 0.92 1.0 0.64 241 W241H 0.65 1.08 0.99 1.12 1.1 1.05 241 W241I 0.75 1.11 0.99 1.13 1.0 1.15 241 W241K 0.83 1.00 0.88 1.22 1.0 1.11 241 W241L 0.85 0.78 1.00 1.03 1.0 0.99 241 W241M 0.91 1.01 0.82 1.04 1.1 1.07 241 W241N 0.35 1.14 0.92 1.07 1.2 0.64 241 W241Q 0.65 1.40 1.00 1.14 1.1 1.14 241 W241R 0.59 0.93 0.88 1.12 0.9 1.37 241 W241S 0.66 1.14 0.68 1.04 0.9 1.06 241 W241T 0.61 1.06 0.86 1.16 1.0 1.11 241 W241V 0.61 1.20 1.01 1.09 1.0 1.35 241 W241Y 0.81 1.17 0.84 1.08 1.0 1.38 242 T242A 1.24 0.92 1.10 0.95 1.1 0.75 242 T242C 1.10 0.89 1.21 0.84 1.1 0.86 242 T242E 1.03 1.08 1.32 0.87 1.0 0.90 242 T242F 0.71 0.86 0.97 0.81 0.9 0.99 242 T242G 0.88 0.74 1.02 1.03 1.0 0.95 242 T242H 0.95 1.14 0.98 0.90 1.1 0.92 242 T242I 0.84 0.82 1.26 1.11 1.1 0.93 242 T242K 0.99 0.77 1.07 0.93 1.1 0.94 242 T242L 0.97 0.99 1.12 1.01 1.1 0.89 242 T242M 1.00 0.83 1.03 0.97 1.0 0.87 242 T242N 1.02 0.65 1.14 0.96 1.1 0.92 242 T242P 0.93 0.83 1.22 1.06 1.1 0.97 242 T242Q 0.91 0.87 1.34 0.95 1.1 1.23 242 T242R 0.91 1.04 1.18 0.91 1.1 1.05 242 T242S 1.05 1.00 1.16 1.18 1.1 0.95 242 T242V 0.80 0.89 1.20 0.99 1.0 1.05 242 T242W 0.62 0.72 0.97 0.91 1.1 0.96 242 T242Y 0.69 0.94 0.97 1.01 1.1 1.02 243 N243C 1.05 0.88 1.22 0.98 1.0 0.93 243 N243E 1.14 0.94 1.22 0.98 1.1 0.79 243 N243F 0.69 0.75 1.03 1.01 0.6 0.79 243 N243G 0.97 1.16 0.94 1.00 1.2 0.72 243 N243I 0.94 0.79 1.61 0.79 0.8 0.91 243 N243K 0.78 0.97 1.05 1.11 0.9 0.85 243 N243L 0.83 0.92 1.24 1.03 0.8 0.74 243 N243Q 0.93 0.74 1.28 1.03 1.0 0.94 243 N243R 0.73 0.79 0.92 0.90 0.8 1.09 243 N243S 0.97 1.05 1.13 0.86 1.0 0.93 243 N243T 0.92 0.97 1.01 0.92 1.0 0.98 243 N243V 0.89 0.87 1.13 1.13 1.0 1.29 243 N243W 0.59 0.90 1.02 1.01 0.6 1.05 243 N243Y 0.81 0.82 1.20 0.82 0.9 0.92 244 T244A 1.53 0.66 0.97 1.07 1.0 0.84 244 T244D 1.13 0.97 1.23 1.13 1.0 1.11 244 T244E 0.69 0.89 1.12 0.90 1.0 0.92 244 T244F 0.83 0.97 0.97 1.01 1.0 0.96 244 T244G 1.05 0.83 1.06 1.01 1.0 0.96 244 T244H 1.06 0.90 1.29 1.01 1.1 0.94 244 T244K 1.09 0.76 0.95 1.00 1.0 0.97 244 T244L 0.99 1.07 1.13 0.92 1.1 1.00 244 T244M 1.15 0.94 1.05 1.07 1.0 0.96 244 T244N 1.03 1.20 1.10 1.03 1.1 0.95 244 T244P 0.74 0.89 1.25 1.00 1.0 1.00 244 T244Q 1.04 0.87 1.23 0.94 1.0 1.08 244 T244R 0.96 0.54 1.04 0.91 0.9 1.10 244 T244S 1.04 1.02 1.23 1.07 1.0 0.99 244 T244V 0.90 0.69 1.07 1.04 1.0 1.06 244 T244W 0.88 0.70 1.29 0.94 1.0 1.13 244 T244Y 0.87 0.38 1.03 1.01 1.0 1.10 245 Q245A 1.00 0.92 1.10 0.93 1.1 0.92 245 Q245C 0.80 0.79 1.15 0.93 1.1 0.89 245 Q245D 1.00 0.73 1.19 0.88 1.1 0.90 245 Q245E 1.03 1.00 1.15 0.79 1.2 0.89 245 Q245F 0.80 0.89 1.21 1.00 1.0 0.98 245 Q245G 0.76 1.12 1.17 0.99 1.1 0.99 245 Q245H 0.93 1.01 1.04 0.97 1.1 0.94 245 Q245I 0.83 0.97 1.12 1.01 1.1 0.99 245 Q245K 0.99 0.83 0.82 0.88 1.1 0.96 245 Q245L 0.88 0.77 1.18 0.85 1.1 0.97 245 Q245M 1.06 0.81 1.19 1.10 1.1 0.92 245 Q245N 0.63 0.91 0.96 0.79 1.0 0.82 245 Q245P 0.27 0.47 0.63 0.50 1.0 0.25 245 Q245R 0.76 0.57 0.89 0.97 1.0 1.07 245 Q245S 0.81 0.93 1.19 0.97 0.9 1.14 245 Q245T 0.82 0.90 1.18 1.03 1.0 1.37 245 Q245V 0.72 0.96 1.19 1.06 1.0 1.09 245 Q245W 0.50 0.94 1.00 0.90 0.9 1.08 245 Q245Y 1.06 0.66 1.08 0.99 1.0 1.06 246 V246A 0.53 1.06 1.22 1.01 0.9 0.92 246 V246C 0.64 0.95 1.05 0.92 1.1 1.02 246 V246F 0.31 1.18 1.59 1.59 0.8 0.81 246 V246I 1.00 1.00 1.11 0.81 1.1 0.95 246 V246L 0.67 1.05 1.10 0.88 1.0 0.94 246 V246N 0.20 0.32 0.16 0.32 1.2 0.08 246 V246S 0.23 0.60 0.54 0.81 0.7 0.33 246 V246T 0.74 0.95 1.23 1.04 1.0 1.10 247 R247A 0.55 0.86 1.05 0.74 0.2 0.70 247 R247C 0.36 1.07 1.40 1.04 0.4 0.64 247 R247D 0.23 0.43 0.88 0.46 0.2 0.15 247 R247E 0.38 0.77 1.02 0.88 0.3 0.59 247 R247F 0.32 0.96 1.09 0.86 0.3 0.65 247 R247H 0.31 1.31 1.51 1.28 0.3 0.68 247 R247I 0.37 1.16 1.37 1.11 0.2 0.88 247 R247K 0.50 1.01 1.17 1.02 0.5 0.75 247 R247L 0.30 1.65 1.54 1.25 0.1 0.55 247 R247M 0.42 1.07 1.22 0.83 0.2 0.63 247 R247S 0.37 1.06 1.56 0.93 0.4 0.74 247 R247T 0.44 1.18 1.33 1.11 0.5 0.97 247 R247V 0.40 0.84 1.31 1.01 0.4 0.76 247 R247W 0.32 1.35 1.39 0.95 0.3 0.68 247 R247Y 0.27 1.53 2.24 1.48 0.2 0.90 248 S248A 1.06 1.03 1.21 1.00 1.0 1.25 248 S248C 1.02 0.82 1.09 0.96 1.0 0.91 248 S248E 1.21 0.61 1.11 0.86 1.0 1.02 248 S248F 0.98 0.97 1.11 0.96 0.9 1.52 248 S248G 0.93 1.11 0.97 0.96 0.9 1.10 248 S248H 0.78 1.16 1.10 0.98 1.0 0.99 248 S248I 1.00 1.01 1.23 1.13 0.9 1.20 248 S248K 1.07 0.54 0.99 1.02 0.9 0.98 248 S248L 1.00 0.82 1.08 1.01 0.9 1.18 248 S248M 1.00 0.75 1.31 0.96 1.0 1.05 248 S248N 1.08 0.96 1.19 1.05 1.0 1.01 248 S248P 0.57 1.06 1.39 1.07 0.9 1.00 248 S248Q 1.10 1.01 1.14 0.84 1.0 0.93 248 S248R 1.10 0.47 0.80 0.87 0.9 0.87 248 S248T 0.95 0.93 1.19 0.96 1.0 1.07 248 S248V 0.80 1.16 1.13 1.01 0.8 1.31 248 S248W 0.85 0.87 1.24 1.02 1.1 0.99 248 S248Y 1.31 0.89 1.17 0.94 1.0 0.98 249 S249A 1.07 0.92 1.25 1.02 1.0 0.95 249 S249C 1.14 0.97 1.21 0.92 1.0 0.86 249 S249D 0.97 0.84 1.17 0.90 0.9 1.27 249 S249F 1.14 0.75 0.97 0.95 0.8 0.89 249 S249G 0.72 0.83 1.17 0.98 0.9 1.04 249 S249H 1.10 0.95 0.87 1.12 0.9 0.87 249 S249I 0.92 0.76 1.30 0.99 0.9 0.93 249 S249K 1.08 0.91 0.83 0.87 0.8 0.93 249 S249L 0.99 0.89 1.19 0.91 0.8 1.21 249 S249M 1.07 0.99 1.24 1.11 1.0 1.00 249 S249N 1.00 1.08 1.35 1.06 1.0 0.92 249 S249Q 1.00 0.73 1.06 1.17 0.8 1.12 249 S249R 1.03 0.78 0.87 0.95 0.9 1.00 249 S249T 1.08 0.78 1.17 0.95 0.9 1.13 249 S249V 0.97 0.82 1.18 1.05 0.9 0.99 249 S249W 0.95 0.92 1.09 1.17 0.8 1.06 249 S249Y 0.94 0.80 1.07 0.91 0.9 1.01 250 L250C 0.37 1.06 1.50 1.21 0.9 1.21 250 L250F 0.61 1.05 1.44 0.90 0.7 0.96 250 L250I 0.98 0.88 1.22 1.00 0.9 1.13 250 L250M 0.90 1.09 1.13 1.20 1.0 1.05 250 L250T 0.25 1.49 2.25 1.69 0.8 0.81 250 L250V 0.80 0.64 1.06 1.02 0.9 0.98 251 E251A 0.93 0.92 0.67 0.98 0.6 0.70 251 E251C 0.66 0.99 1.04 1.14 0.8 0.69 251 E251D 0.76 1.08 1.07 1.12 0.8 0.95 251 E251F 0.68 0.96 0.65 1.04 0.7 0.66 251 E251G 0.65 1.07 0.83 1.17 0.6 0.95 251 E251H 0.64 1.03 0.74 1.04 0.5 0.74 251 E251I 0.58 0.93 0.91 0.93 0.5 0.81 251 E251K 0.62 0.54 0.41 0.89 0.1 0.65 251 E251L 0.60 0.85 0.54 1.04 0.7 0.72 251 E251M 0.65 0.78 0.62 0.87 0.6 0.62 251 E251N 0.69 0.96 0.78 1.09 0.6 0.85 251 E251Q 0.61 1.12 0.91 1.10 0.5 0.77 251 E251R 0.43 0.66 0.74 1.23 0.2 0.79 251 E251S 0.52 0.81 0.99 0.96 0.6 0.81 251 E251T 0.69 1.02 0.91 1.00 0.7 0.93 251 E251V 0.61 1.05 0.78 1.19 0.6 0.88 251 E251W 0.50 1.21 0.90 1.07 0.3 0.73 251 E251Y 0.58 0.92 0.57 0.97 0.4 0.74 252 N252A 1.02 1.03 1.28 0.97 1.0 0.93 252 N252C 1.01 0.91 0.88 1.01 1.1 0.83 252 N252E 0.77 0.94 0.93 1.01 1.1 0.95 252 N252F 0.27 1.07 0.77 1.10 0.9 0.49 252 N252G 0.88 1.23 0.86 1.08 1.1 0.97 252 N252H 0.94 1.17 0.88 1.09 1.1 0.97 252 N252I 0.81 1.07 1.11 0.94 1.0 1.10 252 N252K 1.08 0.87 0.86 0.93 1.0 0.90 252 N252L 0.96 1.09 0.85 1.08 1.0 1.02 252 N252M 0.89 0.98 1.11 1.10 1.1 1.03 252 N252Q 1.37 1.32 1.08 1.09 1.1 0.98 252 N252R 0.95 0.84 0.90 1.08 0.9 0.99 252 N252S 0.95 1.05 1.13 1.03 1.0 1.16 252 N252T 0.81 1.23 1.11 1.18 1.1 1.05 252 N252V 0.74 0.99 0.99 1.28 1.0 1.24 252 N252W 0.80 1.12 1.04 1.10 1.0 1.21 252 N252Y 0.82 1.06 0.93 1.14 1.0 1.09 253 T253A 1.02 0.94 1.16 0.98 0.9 0.82 253 T253C 0.81 0.89 1.19 0.95 1.0 0.86 253 T253D 0.77 1.10 1.02 1.03 0.8 0.78 253 T253E 0.91 1.10 1.08 0.92 1.0 0.87 253 T253F 1.00 1.10 0.88 1.01 1.0 0.82 253 T253G 0.97 0.97 1.04 1.05 0.8 0.86 253 T253H 1.25 0.99 0.94 1.04 1.0 0.89 253 T253I 0.43 1.14 0.91 0.90 0.1 0.66 253 T253K 0.94 0.89 0.83 1.09 0.6 0.88 253 T253L 0.86 1.15 0.85 1.08 0.8 1.00 253 T253M 1.04 0.88 1.05 1.19 0.8 0.84 253 T253N 0.92 1.10 1.14 1.03 1.0 0.88 253 T253Q 0.88 1.05 1.09 1.08 0.8 1.27 253 T253R 0.83 0.70 0.73 1.08 0.4 0.92 253 T253S 1.00 1.13 1.23 1.08 1.0 0.94 253 T253V 0.49 1.28 1.10 1.09 0.2 1.10 253 T253Y 0.21 3.47 2.00 1.61 0.2 0.10 254 T254A 1.14 0.93 1.13 1.00 1.0 0.76 254 T254C 1.01 0.99 1.08 1.14 1.1 0.83 254 T254E 0.25 1.23 1.03 1.06 0.1 0.39 254 T254G 0.55 1.00 1.16 1.13 0.8 0.85 254 T254I 0.48 1.08 1.07 1.16 0.2 0.81 254 T254M 0.27 1.06 0.92 1.30 0.1 0.34 254 T254P 0.83 1.16 0.97 1.07 0.7 0.88 254 T254S 0.93 0.95 1.03 0.90 1.0 0.92 254 T254V 1.00 1.19 0.97 1.07 0.8 1.05 257 L257A 0.72 1.00 1.27 0.91 0.6 0.99 257 L257C 0.78 1.09 1.04 1.05 0.8 0.83 257 L257D 0.37 1.17 1.22 0.83 0.4 0.68 257 L257E 0.50 1.05 1.27 0.92 0.6 0.81 257 L257F 0.67 0.60 1.05 0.91 0.2 0.98 257 L257G 0.67 1.01 0.64 1.20 0.7 0.90 257 L257H 0.56 0.83 1.00 1.01 0.4 0.87 257 L257I 0.83 0.89 1.04 0.97 0.9 1.06 257 L257M 0.84 1.06 0.93 0.86 0.8 0.83 257 L257N 0.52 1.16 1.00 1.00 0.5 0.87 257 L257P 0.45 0.69 0.96 0.91 0.3 0.73 257 L257R 0.59 0.64 0.76 1.04 0.1 0.88 257 L257S 0.62 0.93 1.10 0.97 0.5 1.03 257 L257T 0.62 1.05 1.29 1.00 0.7 1.06 257 L257V 0.76 0.91 0.90 0.97 0.9 0.90 257 L257Y 0.62 1.17 1.00 0.98 0.4 0.84 258 G258A 0.59 1.05 1.13 1.14 0.1 0.61 258 G258C 0.53 0.87 1.15 1.03 0.4 0.62 258 G258E 0.57 0.98 1.11 1.12 0.9 0.71 258 G258I 0.29 1.26 1.39 1.41 0.3 0.53 258 G258M 0.43 1.02 1.05 1.29 0.1 0.63 258 G258Q 0.52 1.05 1.26 1.12 0.4 0.80 258 G258V 0.38 1.26 1.57 1.45 0.6 0.81 261 F261A 0.55 0.82 0.95 0.91 0.5 0.59 261 F261C 0.57 0.80 1.08 0.95 0.7 0.68 261 F261E 0.65 0.65 1.05 0.94 0.7 0.68 261 F261G 0.46 0.75 0.82 0.80 0.2 0.55 261 F261H 0.74 0.92 1.04 0.99 0.8 0.77 261 F261L 0.77 0.84 0.77 0.95 0.8 0.62 261 F261M 0.73 0.79 0.90 0.76 0.7 0.73 261 F261N 0.80 0.92 0.88 0.92 0.8 0.72 261 F261P 0.45 0.87 0.86 0.95 0.3 0.60 261 F261Q 0.57 0.78 1.10 0.95 0.7 0.73 261 F261R 0.58 0.71 0.48 0.93 0.2 0.66 261 F261S 0.54 0.89 0.87 0.98 0.5 0.68 261 F261T 0.56 0.98 1.26 1.25 0.7 0.88 261 F261V 0.57 0.92 1.09 0.87 0.7 0.78 261 F261W 0.89 0.70 0.98 1.18 1.1 0.80 261 F261Y 0.67 0.63 0.94 0.97 0.9 0.79 262 Y262A 0.83 0.81 0.96 0.84 0.5 0.70 262 Y262C 1.10 0.91 0.98 0.83 0.9 0.78 262 Y262D 0.92 0.99 0.91 0.97 0.8 0.61 262 Y262E 0.86 1.01 1.11 1.06 0.9 0.77 262 Y262F 1.11 0.77 1.10 0.93 0.9 0.93 262 Y262G 0.55 0.94 0.60 1.03 0.2 0.56 262 Y262H 0.93 0.81 0.77 1.01 0.9 0.87 262 Y262I 0.72 0.59 0.86 0.90 0.6 0.53 262 Y262K 0.84 0.53 0.67 0.95 0.1 0.96 262 Y262L 0.92 0.96 1.06 0.90 0.9 0.81 262 Y262M 1.00 0.60 0.88 1.02 0.9 0.75 262 Y262N 0.82 1.00 1.13 0.86 0.7 0.77 262 Y262Q 0.82 0.86 0.96 0.91 0.8 0.72 262 Y262S 0.79 1.08 0.91 1.00 0.7 0.80 262 Y262T 0.65 0.94 0.95 0.86 0.7 0.71 262 Y262V 0.51 1.01 0.90 0.94 0.6 0.69 262 Y262W 0.83 0.81 0.99 1.03 0.8 0.89 263 Y263A 0.56 0.84 0.93 0.93 0.1 0.76 263 Y263C 0.98 0.86 0.98 0.93 0.6 0.90 263 Y263D 0.31 1.61 1.44 1.22 0.5 0.71 263 Y263E 0.47 1.02 0.98 0.86 0.5 0.80 263 Y263F 1.03 1.14 0.97 0.89 0.9 0.80 263 Y263K 0.22 2.39 2.76 1.86 0.1 0.34 263 Y263L 0.84 0.89 0.83 0.95 0.2 1.00 263 Y263M 0.96 0.99 1.08 0.97 0.6 0.74 263 Y263R 0.21 8.02 4.08 1.72 0.1 0.26 263 Y263S 0.47 1.06 0.82 0.95 0.2 0.77 263 Y263T 0.91 0.84 0.97 1.10 0.7 0.97 263 Y263V 0.66 0.80 0.89 0.94 0.4 1.07 263 Y263W 0.35 0.96 0.90 0.95 0.1 0.64 264 G264A 0.55 0.81 0.96 0.93 0.3 0.79 265 K265A 1.18 1.03 1.24 0.86 0.8 0.96 265 K265C 0.92 0.96 1.54 1.11 0.9 0.93 265 K265D 0.59 1.05 1.24 0.85 0.9 0.77 265 K265E 0.70 1.00 1.32 0.90 1.0 0.94 265 K265G 0.89 1.22 1.38 1.04 0.7 0.97 265 K265H 0.69 1.16 1.06 0.92 1.1 0.88 265 K265L 0.59 1.11 1.44 1.11 1.2 0.97 265 K265M 0.78 1.04 1.19 0.99 1.0 0.88 265 K265N 1.05 1.07 1.31 1.00 1.2 0.85 265 K265P 0.25 1.61 1.92 1.59 1.0 0.80 265 K265Q 0.76 1.16 1.19 1.03 1.3 0.82 265 K265R 1.16 1.11 0.88 1.17 1.1 0.92 265 K265S 1.06 1.13 1.15 1.04 1.0 0.88 265 K265T 0.80 1.08 1.20 1.01 1.1 0.87 265 K265V 0.51 1.12 1.33 0.96 0.9 0.87 265 K265W 0.75 1.28 1.35 1.08 1.0 1.20 265 K265Y 0.85 1.07 1.25 1.02 1.0 1.26 267 L267A 0.82 1.07 1.22 1.07 0.9 1.10 267 L267C 0.68 1.04 1.22 1.19 0.9 1.14 267 L267E 0.58 1.17 1.35 1.10 1.1 1.19 267 L267F 0.72 0.98 1.11 1.13 0.2 0.81 267 L267G 0.62 0.71 1.13 1.16 0.3 0.97 267 L267H 0.63 1.07 1.21 1.13 0.1 1.05 267 L267I 0.91 1.06 1.25 1.07 1.1 0.99 267 L267M 0.77 0.94 1.22 0.95 0.9 1.00 267 L267Q 0.73 1.14 1.32 1.11 0.9 1.27 267 L267S 0.71 1.03 1.07 1.16 0.5 1.15 267 L267T 0.63 1.19 1.25 1.33 0.5 1.33 267 L267V 0.73 1.12 1.08 1.24 0.8 1.06 268 I268A 0.86 0.85 0.88 0.95 0.7 0.68 268 I268C 0.95 0.94 0.73 1.18 0.9 0.78 268 I268E 0.22 0.83 1.00 0.50 0.5 0.07 268 I268L 0.99 0.85 1.01 1.08 0.7 0.91 268 I268M 0.88 1.03 1.06 1.04 0.3 1.08 268 I268P 0.69 0.69 0.76 0.82 0.4 0.60 268 I268T 0.25 1.90 1.96 1.76 0.8 0.44 268 I268V 0.93 0.95 0.76 1.13 1.0 0.90 269 N269A 0.48 1.02 1.00 1.07 0.3 0.82 269 N269D 1.25 1.14 0.89 1.01 1.3 0.90 269 N269E 0.83 1.26 1.08 1.05 1.1 1.01 269 N269G 0.53 0.88 0.95 1.03 0.1 0.89 269 N269I 0.69 1.00 1.06 1.04 0.6 1.00 269 N269K 0.64 0.75 0.81 1.01 0.5 0.89 269 N269L 0.39 0.88 0.96 1.17 0.1 0.84 269 N269M 0.81 0.88 0.86 0.91 0.5 0.87 269 N269Q 0.84 1.00 0.85 1.19 1.0 0.96 269 N269S 0.94 1.02 1.15 1.12 0.8 1.00 269 N269T 0.56 0.85 0.91 0.91 0.3 0.88 269 N269V 0.44 1.01 0.97 1.24 0.5 0.95 270 V270A 1.21 0.98 1.07 1.02 1.0 0.77 270 V270C 1.09 0.99 1.05 1.03 1.1 0.90 270 V270F 0.17 2.38 2.92 1.13 0.2 0.08 270 V270G 0.41 0.98 0.92 1.09 0.8 0.84 270 V270I 0.88 0.96 1.09 1.01 1.0 0.89 270 V270L 0.90 1.02 1.01 0.87 0.7 0.86 270 V270M 0.81 0.92 1.01 0.94 0.4 0.77 270 V270N 0.64 0.94 1.31 0.89 0.7 0.93 270 V270P 0.50 0.91 1.08 0.93 0.8 0.80 270 V270S 1.08 0.99 0.95 0.78 1.0 0.84 270 V270T 0.94 0.96 1.07 1.01 0.8 1.06 271 Q271A 1.18 0.94 1.12 1.04 1.1 0.83 271 Q271C 0.99 1.02 0.98 1.08 1.2 0.86 271 Q271D 1.00 1.03 0.84 1.00 1.1 0.89 271 Q271E 1.01 0.93 1.16 0.95 1.2 1.02 271 Q271F 1.09 1.04 0.80 1.05 1.0 0.89 271 Q271G 0.92 0.97 0.86 1.06 0.7 0.96 271 Q271H 0.92 1.01 0.85 1.09 1.0 1.04 271 Q271I 1.07 1.04 0.88 0.96 1.0 0.86 271 Q271K 1.03 0.60 0.57 1.09 0.5 1.01 271 Q271L 1.16 0.90 0.94 1.01 1.0 0.88 271 Q271M 1.15 0.89 1.19 1.11 1.0 0.96 271 Q271N 0.99 0.91 0.91 1.09 0.9 1.01 271 Q271P 1.03 0.75 1.12 1.06 1.1 0.76 271 Q271R 1.23 0.63 1.09 1.05 0.2 0.95 271 Q271S 0.97 0.85 1.02 0.98 1.0 0.96 271 Q271T 0.88 0.97 0.91 1.11 0.8 0.99 271 Q271V 0.92 1.06 0.84 1.11 0.9 0.97 271 Q271W 1.00 0.90 0.94 1.14 0.9 1.07 271 Q271Y 0.96 0.94 0.95 0.98 0.9 0.97 272 A272E 1.08 0.82 1.09 0.96 1.1 0.79 272 A272F 0.88 1.02 1.08 0.99 0.9 0.91 272 A272G 1.07 0.79 1.23 1.03 0.8 0.91 272 A272H 1.12 0.90 1.19 1.00 0.9 0.82 272 A272I 0.76 0.72 1.23 0.98 1.0 0.94 272 A272K 1.00 0.61 1.02 0.95 0.9 0.89 272 A272L 0.99 0.87 1.12 0.95 1.1 0.81 272 A272M 0.98 0.77 0.98 1.08 0.9 0.86 272 A272P 0.92 0.93 1.05 0.95 0.8 0.92 272 A272Q 1.19 0.86 1.18 1.02 1.0 0.88 272 A272R 0.99 0.47 0.99 0.81 0.8 1.00 272 A272S 1.00 1.04 1.19 1.09 1.0 0.97 272 A272T 0.88 0.97 0.99 1.04 1.0 1.19 272 A272V 0.80 1.01 1.14 0.99 1.0 1.00 272 A272W 0.91 0.52 1.04 1.07 0.9 1.21 272 A272Y 0.95 0.95 1.28 1.00 1.0 0.93 273 A273E 0.59 0.92 0.99 1.05 0.2 0.57 273 A273G 0.87 0.93 1.21 1.22 0.8 0.94 273 A273H 0.73 1.05 0.98 1.09 0.4 0.75 273 A273L 0.70 0.88 1.13 1.08 0.3 0.71 273 A273N 0.41 1.13 1.13 1.15 0.1 0.66 273 A273Q 0.44 1.09 1.19 1.42 0.1 0.75 273 A273S 0.87 1.06 1.35 1.15 0.7 0.98 273 A273T 0.53 0.79 1.23 1.29 0.2 0.91 273 A273V 0.53 1.41 1.24 1.15 0.3 0.84 274 A274C 0.94 1.10 0.99 0.96 1.0 0.97 274 A274D 0.94 0.92 0.87 0.89 0.7 1.05 274 A274F 0.80 0.82 0.84 0.96 0.6 0.74 274 A274G 0.85 0.94 0.88 0.92 0.9 0.96 274 A274H 0.79 1.17 0.89 0.95 0.5 0.98 274 A274I 0.98 0.99 0.92 1.07 1.0 1.03 274 A274K 0.54 0.94 0.61 0.95 0.2 0.76 274 A274L 0.78 1.21 0.92 1.03 1.1 0.83 274 A274M 0.84 0.87 0.72 0.98 1.0 0.72 274 A274P 0.54 0.99 0.70 1.02 0.4 0.63 274 A274Q 0.77 1.05 0.90 1.07 0.8 0.93 274 A274R 0.41 0.85 0.58 1.12 0.1 1.12 274 A274S 1.12 0.92 0.88 1.05 1.0 0.97 274 A274T 0.91 1.15 0.83 1.06 1.0 1.08 274 A274V 0.96 1.14 0.76 1.19 1.0 1.10 274 A274W 0.37 1.32 0.74 1.09 0.5 0.70 274 A274Y 0.57 1.06 0.86 1.05 0.6 0.93 275 Q275A 0.70 0.95 1.23 0.99 1.0 0.84 275 Q275C 0.41 1.04 1.23 0.91 1.1 0.83 275 Q275D 1.04 1.21 1.03 1.01 1.1 1.08 275 Q275E 1.17 1.01 1.20 1.23 1.1 0.95 275 Q275F 0.70 0.86 0.97 0.89 0.9 1.01 275 Q275G 0.90 0.90 0.81 1.05 1.1 0.77 275 Q275H 1.06 0.79 0.96 1.01 1.1 0.88 275 Q275K 1.02 0.70 0.80 1.06 0.9 0.92 275 Q275L 0.86 0.78 1.01 0.97 1.0 1.00 275 Q275M 0.96 1.16 0.96 0.97 1.0 0.81 275 Q275P 0.74 1.10 1.00 1.00 1.1 0.96 275 Q275R 1.05 0.81 0.80 1.03 0.9 0.97 275 Q275S 0.91 1.12 1.13 1.01 1.0 0.97 275 Q275T 0.85 1.06 1.01 1.05 1.0 0.98 275 Q275V 0.70 1.06 1.09 0.97 1.1 1.07 275 Q275W 0.96 1.02 1.08 1.20 1.0 1.09

Example 7 Comparative Evaluation of Variant Protease Data

In this example, results of experiments conducted to determine cleaning performance, LAS stability, AAPF activity and protein content (tests of properties of interest) of BPN′, GG36 (GCI-P036) and variant proteases are compared. As described throughout functionality of the variant proteases is quantified as a performance index (PI), which is the ratio of performance of a variant to a reference protease. PI classifications used herein include: Up mutations (PI>1.0); Neutral mutations (PI>0.5); Non-deleterious mutations (PI>0.05); and Deleterious mutations (PI≦0.05).

Productive sites are those having at least one Up mutation for any property. Productive, non-restrictive sites are those having >20% neutral mutations (PI>0.5) and at least one Up mutation (PI>1.0) for any property tested (besides protein expression). In Table 7-1 below, the results for variants that meet the definition of a productive, non-restrictive site are shown as a percentage (%) of variants tested that meet the definition of an Up mutation (PI>1).

TABLE 7-1 Productive, Non-Restrictive Sites for BPN′ and GG36 BPN′ BPN′ BPN′ GG36 BPN′ BMI BMI BMI BPN′ GG36 BMI GG36 Position WT # BPN′ BPN′ pH 7/ pH 8/ pH 8/ LAS/ BPN′ WT # GG36 pH 8/ GG36 LAS/ GG36 GG36 (BPN′ #) Residue Variants TCA 16° C. 16° C. 32° EDTA AAPF Residue Variants 32° C. Egg EDTA AAPF TCA 1 A 19 63 21 47 32 26 32 A 16 44 38 6 94 88 2 Q 19 11 32 26 58 0 0 Q 15 20 73 0 100 100 3 S 19 84 21 32 32 21 26 S 15 13 20 20 100 100 4 V 19 26 26 74 26 5 42 V 15 33 53 0 93 93 5 P 19 0 42 37 42 0 11 P 16 56 56 0 38 44 6 Y 19 58 63 37 11 11 11 W 13 31 0 0 0 0 7 G 15 0 7 7 27 0 0 G 18 22 28 0 39 39 8 V 16 0 38 13 75 0 0 I 14 29 36 7 43 43 9 S 19 74 11 11 5 16 42 S 16 75 63 19 88 63 10 Q 19 74 11 21 11 5 26 R 17 88 47 29 41 35 11 I 19 16 37 26 21 5 16 V 15 53 33 0 27 27 12 K 19 79 11 16 16 79 16 Q 16 69 63 25 69 69 13 A 19 11 37 21 16 11 11 A 13 31 31 0 31 23 14 P 19 68 0 63 16 0 79 P 15 73 100 7 73 53 15 A 19 79 0 0 26 42 21 A 13 23 31 54 100 100 16 L 19 32 5 79 58 11 11 A 15 60 33 7 47 47 17 H 19 26 11 42 47 0 5 H 16 56 56 13 63 31 18 S 19 89 0 84 37 32 5 N 19 47 58 32 95 89 19 Q 19 21 42 26 11 21 42 R 18 89 44 89 83 67 20 G 19 16 0 84 58 21 26 G 16 19 13 50 100 94 21 Y 17 41 0 6 35 35 12 L 17 29 18 12 94 82 22 T 18 78 44 0 78 83 39 T 15 33 40 53 93 93 24 S 16 56 75 13 81 88 50 S 16 31 56 75 94 94 25 N 19 47 0 84 63 37 37 G 15 80 80 67 87 47 26 V 17 6 35 12 76 59 18 V 12 33 42 17 83 75 27 K 19 21 11 84 42 58 42 K 17 65 29 47 82 65 28 V 16 13 38 25 56 44 6 V 13 54 15 31 23 23 29 A 17 0 35 29 35 18 12 A 16 38 25 6 13 0 30 V 18 11 50 50 50 17 0 V 14 50 21 29 0 29 31 I 19 11 68 58 58 79 53 L 13 31 31 15 46 38 33 S 15 0 60 0 20 7 7 T 18 61 28 11 6 28 34 G 19 0 5 11 5 0 0 G 15 13 0 0 0 0 35 I 19 0 5 53 47 0 11 I 11 82 27 9 27 27 36 D 18 11 17 11 22 0 0 S 17 47 24 12 65 76 37 S 19 47 58 26 5 16 37 — — — — — — — 38 S 19 74 42 53 74 68 16 T 14 29 29 43 93 79 39 H 19 5 11 53 47 0 26 H 17 53 6 0 6 0 40 P 19 47 74 74 84 16 89 P 17 53 100 29 100 82 41 D 19 0 37 16 26 0 0 D 18 17 6 0 6 6 42 L 19 5 16 16 26 0 5 L 18 50 17 0 39 28 43 K 19 16 0 74 0 74 79 N 16 31 25 63 100 81 44 V 19 0 21 74 68 0 16 I 17 24 24 47 88 94 45 A 16 81 31 6 31 81 94 R 18 78 22 89 89 89 46 G 17 0 59 18 59 18 41 G 17 71 18 94 65 71 47 G 19 0 26 42 68 5 0 G 15 80 53 0 13 20 48 A 17 65 35 12 29 65 24 A 17 76 35 76 88 94 49 S 18 0 22 22 39 6 0 S 12 92 33 25 8 8 50 M 17 6 82 6 41 65 65 F 11 64 45 73 36 45 51 V 19 0 42 68 63 26 0 V 11 73 9 18 55 55 52 P 19 0 74 95 89 5 0 P 16 75 100 38 94 69 53 S 19 74 37 63 26 53 16 G 17 53 12 12 76 82 54 E 19 0 53 53 47 0 0 E 18 28 17 22 39 78 55 T 19 53 21 42 0 79 47 P 18 56 22 33 72 83 56 N 19 5 68 74 63 5 0 S 15 67 40 33 60 73 57 P 19 5 68 84 63 0 0 T 18 44 44 39 100 83 58 F 19 11 63 89 32 11 16 — — — — — — — 59 Q 19 68 68 84 53 47 16 Q 18 44 22 11 78 78 60 D 19 5 5 58 32 0 0 D 17 88 53 0 0 0 61 N 19 100 53 53 21 68 68 G 15 47 27 87 100 73 62 N 19 74 58 42 26 74 16 N 16 75 69 31 75 94 63 S 19 89 47 21 21 32 32 G 16 81 31 0 31 50 66 T 19 5 0 0 0 0 0 T 14 71 7 7 7 7 67 H 14 79 0 0 0 0 0 H 17 18 0 0 0 53 68 V 19 26 42 26 26 11 0 V 19 26 5 0 0 53 69 A 19 0 58 11 26 5 5 A 18 67 17 0 11 6 71 T 19 5 32 47 47 0 5 T 18 67 39 0 11 17 72 V 17 6 65 71 53 6 0 I 16 50 38 13 31 31 73 A 17 6 59 59 65 0 18 A 14 57 71 7 71 36 74 A 19 11 68 5 11 0 0 A 15 13 13 0 13 13 75 L 19 32 11 11 63 0 68 L 17 100 88 0 76 24 76 N 19 32 11 5 42 5 58 N 16 38 63 6 75 63 77 N 19 0 63 11 21 0 0 N 17 88 6 0 6 0 78 S 19 84 74 16 26 42 32 S 18 67 89 44 94 72 79 I 19 74 0 74 42 5 21 I 17 71 71 0 94 53 80 G 19 0 11 21 32 0 0 G 12 92 0 0 0 0 81 V 19 16 79 5 74 0 0 V 18 72 44 0 22 39 82 L 18 0 78 72 83 0 17 L 16 56 69 0 44 38 84 V 19 21 0 0 5 0 26 V 16 56 31 0 44 38 85 A 15 0 20 13 7 0 0 A 11 18 18 0 0 0 86 P 14 0 79 71 93 0 57 P 13 77 62 15 46 15 87 S 16 69 94 38 69 25 25 S 14 50 50 14 93 86 88 A 16 0 69 88 50 6 44 A 14 71 43 0 43 7 89 S 19 5 58 74 53 16 32 E 17 71 76 12 71 41 90 L 14 0 79 71 71 7 14 L 16 56 31 13 38 31 91 Y 19 5 26 74 63 58 5 Y 15 93 67 47 47 33 92 A 15 7 53 53 60 7 0 A 17 94 35 12 18 24 93 V 15 0 40 40 40 20 7 V 16 38 19 56 19 19 94 K 16 0 25 44 19 13 0 K 18 67 11 0 0 11 95 V 18 6 17 6 11 17 11 V 18 56 11 22 11 22 96 L 17 0 71 29 53 12 0 L 16 13 25 31 13 75 97 G 17 35 94 53 94 59 6 G 18 50 50 67 61 89 98 A 19 42 0 63 63 32 47 A 15 60 53 60 93 73 99 D 18 11 83 0 61 50 0 S 14 50 36 50 71 79 100 G 19 16 79 68 79 21 0 G 16 19 25 56 19 81 101 S 16 56 100 19 50 75 56 S 17 47 76 88 76 88 102 G 14 7 29 14 14 14 0 G 16 50 19 19 0 19 103 Q 16 50 63 38 19 69 19 S 16 50 50 56 56 63 104 Y 17 0 47 59 65 47 6 V 15 40 47 60 53 53 105 S 19 0 47 42 32 53 11 S 19 53 26 37 63 53 106 W 19 0 74 63 74 26 0 S 14 64 57 71 71 57 107 I 15 0 40 33 27 13 7 I 18 11 61 6 11 56 108 I 19 5 37 42 32 5 0 A 16 19 38 0 13 19 109 N 19 11 32 11 68 58 42 Q 18 50 78 39 78 39 110 G 16 0 19 25 19 0 0 G 17 6 6 0 6 6 111 I 19 5 37 21 42 11 0 L 16 44 25 6 0 13 112 E 19 0 42 21 53 63 0 E 17 76 29 24 18 12 113 W 19 0 5 42 21 26 0 W 13 0 0 46 0 0 114 A 18 0 33 33 33 11 17 A 11 18 18 9 9 9 115 I 19 0 79 42 79 26 16 G 17 53 76 18 94 82 116 A 19 53 47 42 47 26 74 N 14 86 43 29 100 79 117 N 19 5 53 47 68 58 47 N 11 64 73 73 73 45 118 N 19 32 26 42 32 58 68 G 17 76 88 76 47 47 119 M 18 0 50 56 28 33 17 M 13 46 23 69 23 15 120 D 19 47 47 68 37 68 5 H 13 69 92 69 100 85 121 V 19 5 5 16 5 21 0 V 15 80 33 27 53 40 122 I 19 0 42 42 47 32 5 A 12 58 50 0 25 33 123 N 19 0 58 58 47 0 0 N 12 17 8 0 0 42 124 M 18 17 50 44 39 11 0 L 12 50 25 0 8 17 126 L 14 21 57 36 43 14 0 L 18 0 11 22 0 83 127 G 17 53 24 0 0 0 0 G 12 8 42 8 0 67 128 G 17 12 41 35 29 6 0 S 17 18 24 82 59 94 129 P 19 58 63 37 53 16 32 P 14 21 7 7 100 93 130 S 19 74 11 16 11 53 42 S 10 30 40 40 80 90 131 G 19 5 0 32 11 16 32 P 12 58 17 17 58 83 132 S 19 5 53 53 47 16 0 S 12 75 75 8 58 25 133 A 19 21 21 5 0 63 58 A 10 60 30 50 80 80 134 A 19 0 42 26 26 58 21 T 12 67 25 25 17 8 135 L 13 8 62 46 46 15 0 L 13 54 8 8 15 15 136 K 19 5 68 42 26 21 26 E 17 12 47 0 41 35 137 A 19 21 47 16 16 53 89 Q 13 62 69 38 77 69 138 A 19 0 63 53 74 0 32 A 14 43 29 14 0 7 139 V 19 5 16 16 32 11 11 V 15 73 27 0 13 13 140 D 19 5 5 11 0 0 21 N 17 82 53 6 76 65 141 K 19 21 21 89 79 74 79 S 13 54 54 46 69 77 142 A 19 0 42 32 32 5 26 A 19 58 37 0 21 11 143 V 19 16 11 47 37 26 47 T 15 73 33 7 80 60 144 A 19 53 68 16 26 42 58 S 18 50 39 33 78 67 145 S 19 47 16 84 74 53 74 R 17 82 65 53 41 35 146 G 19 5 32 74 47 21 58 G 17 88 29 6 12 6 147 V 16 6 88 94 50 56 38 V 12 42 8 8 33 33 148 V 17 0 47 65 65 18 6 L 18 56 39 0 56 39 149 V 16 0 44 69 63 88 19 V 17 71 18 24 24 6 150 V 18 0 17 44 50 28 11 V 14 64 29 0 29 14 151 A 17 0 18 35 35 6 0 A 13 15 8 0 8 31 152 A 15 40 7 7 13 0 0 A 13 8 8 0 0 23 153 A 19 0 26 26 21 0 0 S 13 23 0 0 15 31 154 G 19 0 0 0 0 0 0 G 16 0 6 0 0 0 155 N 17 35 0 0 0 0 0 N 14 0 0 0 0 79 156 E 16 44 0 0 6 13 56 S 18 33 11 0 11 61 157 G 19 0 5 0 0 0 0 G 14 0 0 0 0 14 158 T 19 16 74 16 16 16 11 A 14 29 21 36 86 93 159 S 19 37 74 63 63 32 21 — — — — — — — 160 G 19 11 11 53 11 5 5 — — — — — — — 161 S 19 53 58 74 32 37 47 — — — — — — — 162 S 19 32 63 11 16 37 37 — — — — — — — 163 S 19 5 21 5 5 0 0 G 17 35 29 18 47 47 164 T 17 0 12 29 29 0 0 S 15 27 27 53 87 87 165 V 15 0 7 13 33 7 0 I 17 6 12 6 6 59 166 G 16 63 0 6 6 69 0 S 16 38 38 19 6 75 167 Y 19 5 58 84 74 0 0 Y 19 32 0 0 11 47 169 G 18 6 11 6 11 6 6 A 19 11 16 0 0 11 170 K 18 11 100 83 50 11 11 R 14 93 21 29 21 21 171 Y 18 0 33 22 33 0 0 Y 19 63 32 0 16 11 172 P 17 0 88 71 76 24 76 A 16 56 56 25 94 81 173 S 19 0 68 37 74 5 26 N 19 32 37 16 63 79 174 V 19 0 32 21 42 0 16 A 18 17 17 6 17 22 175 I 19 0 42 26 37 5 11 M 16 50 38 0 50 38 176 A 19 5 11 5 21 11 5 A 16 19 13 0 13 38 177 V 19 0 5 11 26 0 0 V 17 18 12 0 24 24 178 G 17 0 0 6 12 0 0 G 16 6 6 0 6 6 179 A 19 0 11 5 16 0 0 A 14 14 7 0 0 0 180 V 19 11 32 16 53 0 16 T 15 47 7 0 20 20 181 D 19 5 5 5 32 0 16 D 12 0 33 0 8 8 182 S 19 32 53 79 42 16 53 Q 18 17 33 11 100 100 183 S 19 53 42 58 42 32 42 N 17 18 29 6 94 88 184 N 19 5 53 74 47 11 53 N 18 61 11 6 6 6 185 Q 19 11 47 63 53 16 84 N 17 41 24 24 94 88 186 R 19 0 89 95 79 5 0 R 17 53 12 24 12 6 187 A 19 11 68 74 26 0 11 A 19 5 16 0 5 37 188 S 19 47 32 84 26 11 32 S 16 6 0 19 100 100 189 F 17 29 24 12 29 0 0 F 16 6 0 0 0 88 190 S 19 0 21 26 16 0 0 S 19 0 0 0 0 84 191 Q 19 5 5 11 11 0 0 Q 16 6 0 13 0 75 192 Y 19 0 32 53 26 0 5 Y 17 6 12 6 0 53 193 G 19 0 21 11 0 0 0 G 15 0 0 0 0 87 194 P 19 0 74 47 68 0 68 A 17 18 35 35 94 94 195 E 19 0 32 11 21 0 0 G 16 56 44 13 13 19 196 L 19 0 21 21 26 5 5 L 14 21 14 0 7 43 197 D 15 0 27 40 47 0 0 D 18 83 50 0 44 39 198 V 18 0 6 33 33 11 17 I 17 41 12 0 59 59 199 M 18 0 50 28 33 0 6 V 17 47 29 12 29 29 200 A 19 0 42 16 32 0 16 A 11 36 27 0 18 18 201 P 18 0 44 44 78 0 22 P 16 31 13 0 0 0 203 V 18 0 33 78 67 17 50 V 16 75 19 13 19 25 204 S 16 0 13 38 0 31 44 N 14 14 29 7 93 93 205 I 19 0 16 11 32 5 11 V 15 33 13 13 7 13 206 Q 19 68 53 32 84 26 16 Q 18 67 28 17 94 44 207 S 19 0 5 5 0 0 0 S 18 11 11 0 6 0 208 T 19 0 37 37 37 0 21 T 18 39 22 0 22 11 209 L 19 5 32 21 37 0 32 Y 18 83 67 0 89 44 210 P 19 0 74 42 68 0 11 P 17 100 100 29 94 24 211 G 19 5 79 79 53 21 37 G 15 53 67 20 93 93 212 N 19 26 42 42 32 5 16 S 13 46 46 38 92 92 213 K 17 47 94 100 18 94 29 T 18 22 39 6 94 94 214 Y 18 0 72 50 44 0 0 Y 18 100 39 0 22 17 215 G 19 11 68 26 32 11 0 A 17 71 59 41 100 94 216 A 19 42 32 42 37 53 21 S 18 56 72 33 100 100 217 Y 19 32 47 26 58 53 58 L 16 50 81 25 6 19 218 N 19 5 26 11 16 16 32 N 17 76 76 24 88 35 219 G 19 5 0 0 0 16 0 G 16 0 0 0 0 6 220 T 19 0 5 5 5 0 0 T 15 7 7 0 0 33 222 M 18 67 0 0 17 28 6 M 17 6 12 12 0 94 223 A 19 5 11 0 0 0 0 A 18 11 6 0 6 17 224 S 19 11 37 26 42 5 5 T 17 29 18 12 18 35 225 P 19 16 0 0 0 0 0 P 18 0 6 11 0 33 226 H 19 0 58 53 63 0 16 H 16 75 44 0 6 6 227 V 19 5 32 47 26 5 0 V 16 50 25 0 44 44 228 A 16 0 25 25 38 6 0 A 17 18 6 12 29 24 229 G 19 5 0 5 5 0 5 G 15 20 13 0 13 7 230 A 19 11 21 47 58 11 21 A 16 81 50 6 69 44 231 A 19 0 47 58 58 5 5 A 16 19 25 6 50 50 232 A 13 0 38 54 23 38 15 A 10 60 30 20 30 20 233 L 11 0 18 36 18 27 0 L 16 94 81 6 75 31 234 I 19 32 37 32 26 21 32 V 12 58 33 8 75 75 235 L 19 47 32 37 47 68 32 K 16 88 63 56 88 88 236 S 19 42 32 21 32 26 42 Q 16 94 88 13 75 50 237 K 19 79 26 37 26 37 58 K 17 94 71 65 88 82 238 H 19 0 37 47 42 58 26 N 17 71 71 47 94 88 239 P 19 0 58 16 47 84 53 P 17 71 82 65 100 82 240 N 19 42 68 11 47 79 42 S 14 71 93 14 93 79 241 W 19 0 68 21 79 63 58 W 19 42 63 63 95 84 242 T 19 32 16 74 32 89 21 S 15 33 33 47 100 73 243 N 19 11 11 63 37 21 16 N 18 39 50 39 94 89 244 T 19 47 16 74 53 68 37 V 16 56 75 63 94 81 245 Q 19 16 11 79 26 84 32 Q 13 62 77 46 100 77 246 V 17 6 18 35 18 18 12 I 17 76 24 29 35 35 247 R 19 0 53 74 42 0 0 R 19 53 68 21 84 79 248 S 19 47 37 79 42 32 58 N 16 69 56 31 94 88 249 S 19 42 5 68 37 5 42 H 18 17 28 39 94 83 250 L 19 0 26 32 26 0 16 L 17 65 12 0 29 24 251 E 19 0 37 11 63 0 0 K 14 64 50 50 86 64 252 N 19 21 58 37 74 53 42 N 16 38 81 63 88 75 253 T 19 16 53 58 68 11 16 T 14 36 29 7 93 79 254 T 19 16 53 47 63 11 5 A 18 39 22 0 22 11 255 T 19 26 58 53 37 0 42 T 17 18 29 35 94 94 256 K 19 11 89 95 58 0 68 S 17 47 82 35 100 65 257 L 19 0 47 53 32 0 16 L 15 87 40 0 40 13 258 G 17 0 47 82 94 0 0 G 17 82 59 0 82 53 259 D 19 21 5 0 11 0 89 S 12 83 100 8 100 25 260 S 19 26 63 63 37 0 47 T 14 64 86 21 100 79 261 F 19 0 0 32 11 5 0 N 16 56 88 63 100 75 262 Y 19 11 26 26 37 0 0 L 17 71 71 35 94 88 263 Y 19 5 37 32 26 0 5 Y 15 93 33 0 13 7 264 G 19 0 5 5 16 0 0 G 14 79 7 0 7 0 265 K 19 21 84 84 58 47 11 S 18 83 83 6 72 44 266 G 19 0 0 5 5 0 0 G 17 6 0 0 0 0 267 L 18 0 61 83 89 11 56 L 17 76 41 0 41 6 268 I 19 0 26 37 37 0 5 V 15 53 13 0 53 47 269 N 19 5 32 26 63 11 5 N 13 85 85 8 100 69 270 V 18 17 11 50 33 17 6 A 17 88 71 0 65 35 271 Q 19 53 32 32 79 47 26 E 14 29 100 0 100 64 272 A 19 26 16 68 32 37 16 A 16 69 63 25 100 69 273 A 13 0 69 85 100 0 0 A 15 100 73 7 73 27 274 A 19 5 42 0 53 16 26 T 15 87 80 13 87 60 275 Q 19 26 47 53 47 58 26 R 14 86 50 79 71 50

Highly productive sites are those having ≧20% Up mutations (PI>1) for at least one property other than protein expression (TCA assay). In Table 7-2 below, the results for variants that meet the definition of a highly productive site are shown as a percentage (%) of variants tested that meet the definition of an Up mutation (PI>1).

TABLE 7-2 Highly Productive Sites for BPN′ and GG36 BPN′ BPN′ BPN′ GG36 BPN′ BMI BMI BMI GG36 BMI GG36 Position WT # BPN′ BPN′ pH 7/ pH 8/ pH 8/ BPN′ BPN′ WT # GG36 pH 8/ GG36 LAS/ GG36 GG36 (BPN′ #) Residue Variants TCA 16° C. 16° C. 32° LAS AAPF Residue Variants 32° C. Egg EDTA AAPF TCA 1 A 19 63 21 47 32 26 32 A 16 44 38 6 94 88 2 Q 19 11 32 26 58 0 0 Q 15 20 73 0 100 100 3 S 19 84 21 32 32 21 26 S 15 13 20 20 100 100 4 V 19 26 26 74 26 5 42 V 15 33 53 0 93 93 5 P 19 0 42 37 42 0 11 P 16 56 56 0 38 44 6 Y 19 58 63 37 11 11 11 W 13 31 0 0 0 0 7 G 15 0 7 7 27 0 0 G 18 22 28 0 39 39 8 V 16 0 38 13 75 0 0 I 14 29 36 7 43 43 9 S 19 74 11 11 5 16 42 S 16 75 63 19 88 63 10 Q 19 74 11 21 11 5 26 R 17 88 47 29 41 35 11 I 19 16 37 26 21 5 16 V 15 53 33 0 27 27 12 K 19 79 11 16 16 79 16 Q 16 69 63 25 69 69 13 A 19 11 37 21 16 11 11 A 13 31 31 0 31 23 14 P 19 68 0 63 16 0 79 P 15 73 100 7 73 53 15 A 19 79 0 0 26 42 21 A 13 23 31 54 100 100 16 L 19 32 5 79 58 11 11 A 15 60 33 7 47 47 17 H 19 26 11 42 47 0 5 H 16 56 56 13 63 31 18 S 19 89 0 84 37 32 5 N 19 47 58 32 95 89 19 Q 19 21 42 26 11 21 42 R 18 89 44 89 83 67 20 G 19 16 0 84 58 21 26 G 16 19 13 50 100 94 21 Y 17 41 0 6 35 35 12 L 17 29 18 12 94 82 22 T 18 78 44 0 78 83 39 T 15 33 40 53 93 93 24 S 16 56 75 13 81 88 50 S 16 31 56 75 94 94 25 N 19 47 0 84 63 37 37 G 15 80 80 67 87 47 26 V 17 6 35 12 76 59 18 V 12 33 42 17 83 75 27 K 19 21 11 84 42 58 42 K 17 65 29 47 82 65 28 V 16 13 38 25 56 44 6 V 13 54 15 31 23 23 29 A 17 0 35 29 35 18 12 A 16 38 25 6 13 0 30 V 18 11 50 50 50 17 0 V 14 50 21 29 0 29 31 I 19 11 68 58 58 79 53 L 13 31 31 15 46 38 33 S 15 0 60 0 20 7 7 T 18 61 28 11 6 28 35 I 19 0 5 53 47 0 11 I 11 82 27 9 27 27 36 D 18 11 17 11 22 0 0 S 17 47 24 12 65 76 37 S 19 47 58 26 5 16 37 — — — — — — — 38 S 19 74 42 53 74 68 16 T 14 29 29 43 93 79 39 H 19 5 11 53 47 0 26 H 17 53 6 0 6 0 40 P 19 47 74 74 84 16 89 P 17 53 100 29 100 82 41 D 19 0 37 16 26 0 0 D 18 17 6 0 6 6 42 L 19 5 16 16 26 0 5 L 18 50 17 0 39 28 43 K 19 16 0 74 0 74 79 N 16 31 25 63 100 81 44 V 19 0 21 74 68 0 16 I 17 24 24 47 88 94 45 A 16 81 31 6 31 81 94 R 18 78 22 89 89 89 46 G 17 0 59 18 59 18 41 G 17 71 18 94 65 71 47 G 19 0 26 42 68 5 0 G 15 80 53 0 13 20 48 A 17 65 35 12 29 65 24 A 17 76 35 76 88 94 49 S 18 0 22 22 39 6 0 S 12 92 33 25 8 8 50 M 17 6 82 6 41 65 65 F 11 64 45 73 36 45 51 V 19 0 42 68 63 26 0 V 11 73 9 18 55 55 52 P 19 0 74 95 89 5 0 P 16 75 100 38 94 69 53 S 19 74 37 63 26 53 16 G 17 53 12 12 76 82 54 E 19 0 53 53 47 0 0 E 18 28 17 22 39 78 55 T 19 53 21 42 0 79 47 P 18 56 22 33 72 83 56 N 19 5 68 74 63 5 0 S 15 67 40 33 60 73 57 P 19 5 68 84 63 0 0 T 18 44 44 39 100 83 58 F 19 11 63 89 32 11 16 — — — — — — — 59 Q 19 68 68 84 53 47 16 Q 18 44 22 11 78 78 60 D 19 5 5 58 32 0 0 D 17 88 53 0 0 0 61 N 19 100 53 53 21 68 68 G 15 47 27 87 100 73 62 N 19 74 58 42 26 74 16 N 16 75 69 31 75 94 63 S 19 89 47 21 21 32 32 G 16 81 31 0 31 50 66 T 19 5 0 0 0 0 0 T 14 71 7 7 7 7 67 H 14 79 0 0 0 0 0 H 17 18 0 0 0 53 68 V 19 26 42 26 26 11 0 V 19 26 5 0 0 53 69 A 19 0 58 11 26 5 5 A 18 67 17 0 11 6 71 T 19 5 32 47 47 0 5 T 18 67 39 0 11 17 72 V 17 6 65 71 53 6 0 I 16 50 38 13 31 31 73 A 17 6 59 59 65 0 18 A 14 57 71 7 71 36 74 A 19 11 68 5 11 0 0 A 15 13 13 0 13 13 75 L 19 32 11 11 63 0 68 L 17 100 88 0 76 24 76 N 19 32 11 5 42 5 58 N 16 38 63 6 75 63 77 N 19 0 63 11 21 0 0 N 17 88 6 0 6 0 78 S 19 84 74 16 26 42 32 S 18 67 89 44 94 72 79 I 19 74 0 74 42 5 21 I 17 71 71 0 94 53 80 G 19 0 11 21 32 0 0 G 12 92 0 0 0 0 81 V 19 16 79 5 74 0 0 V 18 72 44 0 22 39 82 L 18 0 78 72 83 0 17 L 16 56 69 0 44 38 84 V 19 21 0 0 5 0 26 V 16 56 31 0 44 38 85 A 15 0 20 13 7 0 0 A 11 18 18 0 0 0 86 P 14 0 79 71 93 0 57 P 13 77 62 15 46 15 87 S 16 69 94 38 69 25 25 S 14 50 50 14 93 86 88 A 16 0 69 88 50 6 44 A 14 71 43 0 43 7 89 S 19 5 58 74 53 16 32 E 17 71 76 12 71 41 90 L 14 0 79 71 71 7 14 L 16 56 31 13 38 31 91 Y 19 5 26 74 63 58 5 Y 15 93 67 47 47 33 92 A 15 7 53 53 60 7 0 A 17 94 35 12 18 24 93 V 15 0 40 40 40 20 7 V 16 38 19 56 19 19 94 K 16 0 25 44 19 13 0 K 18 67 11 0 0 11 95 V 18 6 17 6 11 17 11 V 18 56 11 22 11 22 96 L 17 0 71 29 53 12 0 L 16 13 25 31 13 75 97 G 17 35 94 53 94 59 6 G 18 50 50 67 61 89 98 A 19 42 0 63 63 32 47 A 15 60 53 60 93 73 99 D 18 11 83 0 61 50 0 S 14 50 36 50 71 79 100 G 19 16 79 68 79 21 0 G 16 19 25 56 19 81 101 S 16 56 100 19 50 75 56 S 17 47 76 88 76 88 102 G 14 7 29 14 14 14 0 G 16 50 19 19 0 19 103 Q 16 50 63 38 19 69 19 S 16 50 50 56 56 63 104 Y 17 0 47 59 65 47 6 V 15 40 47 60 53 53 105 S 19 0 47 42 32 53 11 S 19 53 26 37 63 53 106 W 19 0 74 63 74 26 0 S 14 64 57 71 71 57 107 I 15 0 40 33 27 13 7 I 18 11 61 6 11 56 108 I 19 5 37 42 32 5 0 A 16 19 38 0 13 19 109 N 19 11 32 11 68 58 42 Q 18 50 78 39 78 39 110 G 16 0 19 25 19 0 0 G 17 6 6 0 6 6 111 I 19 5 37 21 42 11 0 L 16 44 25 6 0 13 112 E 19 0 42 21 53 63 0 E 17 76 29 24 18 12 113 W 19 0 5 42 21 26 0 W 13 0 0 46 0 0 114 A 18 0 33 33 33 11 17 A 11 18 18 9 9 9 115 I 19 0 79 42 79 26 16 G 17 53 76 18 94 82 116 A 19 53 47 42 47 26 74 N 14 86 43 29 100 79 117 N 19 5 53 47 68 58 47 N 11 64 73 73 73 45 118 N 19 32 26 42 32 58 68 G 17 76 88 76 47 47 119 M 18 0 50 56 28 33 17 M 13 46 23 69 23 15 120 D 19 47 47 68 37 68 5 H 13 69 92 69 100 85 121 V 19 5 5 16 5 21 0 V 15 80 33 27 53 40 122 I 19 0 42 42 47 32 5 A 12 58 50 0 25 33 123 N 19 0 58 58 47 0 0 N 12 17 8 0 0 42 124 M 18 17 50 44 39 11 0 L 12 50 25 0 8 17 126 L 14 21 57 36 43 14 0 L 18 0 11 22 0 83 127 G 17 53 24 0 0 0 0 G 12 8 42 8 0 67 128 G 17 12 41 35 29 6 0 S 17 18 24 82 59 94 129 P 19 58 63 37 53 16 32 P 14 21 7 7 100 93 130 S 19 74 11 16 11 53 42 S 10 30 40 40 80 90 131 G 19 5 0 32 11 16 32 P 12 58 17 17 58 83 132 S 19 5 53 53 47 16 0 S 12 75 75 8 58 25 133 A 19 21 21 5 0 63 58 A 10 60 30 50 80 80 134 A 19 0 42 26 26 58 21 T 12 67 25 25 17 8 135 L 13 8 62 46 46 15 0 L 13 54 8 8 15 15 136 K 19 5 68 42 26 21 26 E 17 12 47 0 41 35 137 A 19 21 47 16 16 53 89 Q 13 62 69 38 77 69 138 A 19 0 63 53 74 0 32 A 14 43 29 14 0 7 139 V 19 5 16 16 32 11 11 V 15 73 27 0 13 13 140 D 19 5 5 11 0 0 21 N 17 82 53 6 76 65 141 K 19 21 21 89 79 74 79 S 13 54 54 46 69 77 142 A 19 0 42 32 32 5 26 A 19 58 37 0 21 11 143 V 19 16 11 47 37 26 47 T 15 73 33 7 80 60 144 A 19 53 68 16 26 42 58 S 18 50 39 33 78 67 145 S 19 47 16 84 74 53 74 R 17 82 65 53 41 35 146 G 19 5 32 74 47 21 58 G 17 88 29 6 12 6 147 V 16 6 88 94 50 56 38 V 12 42 8 8 33 33 148 V 17 0 47 65 65 18 6 L 18 56 39 0 56 39 149 V 16 0 44 69 63 88 19 V 17 71 18 24 24 6 150 V 18 0 17 44 50 28 11 V 14 64 29 0 29 14 151 A 17 0 18 35 35 6 0 A 13 15 8 0 8 31 152 A 15 40 7 7 13 0 0 A 13 8 8 0 0 23 153 A 19 0 26 26 21 0 0 S 13 23 0 0 15 31 155 N 17 35 0 0 0 0 0 N 14 0 0 0 0 79 156 E 16 44 0 0 6 13 56 S 18 33 11 0 11 61 158 T 19 16 74 16 16 16 11 A 14 29 21 36 86 93 159 S 19 37 74 63 63 32 21 — — — — — — — 160 G 19 11 11 53 11 5 5 — — — — — — — 161 S 19 53 58 74 32 37 47 — — — — — — — 162 S 19 32 63 11 16 37 37 — — — — — — — 163 S 19 5 21 5 5 0 0 G 17 35 29 18 47 47 164 T 17 0 12 29 29 0 0 S 15 27 27 53 87 87 165 V 15 0 7 13 33 7 0 I 17 6 12 6 6 59 166 G 16 63 0 6 6 69 0 S 16 38 38 19 6 75 167 Y 19 5 58 84 74 0 0 Y 19 32 0 0 11 47 170 K 18 11 100 83 50 11 11 R 14 93 21 29 21 21 171 Y 18 0 33 22 33 0 0 Y 19 63 32 0 16 11 172 P 17 0 88 71 76 24 76 A 16 56 56 25 94 81 173 S 19 0 68 37 74 5 26 N 19 32 37 16 63 79 174 V 19 0 32 21 42 0 16 A 18 17 17 6 17 22 175 I 19 0 42 26 37 5 11 M 16 50 38 0 50 38 176 A 19 5 11 5 21 11 5 A 16 19 13 0 13 38 177 V 19 0 5 11 26 0 0 V 17 18 12 0 24 24 180 V 19 11 32 16 53 0 16 T 15 47 7 0 20 20 181 D 19 5 5 5 32 0 16 D 12 0 33 0 8 8 182 S 19 32 53 79 42 16 53 Q 18 17 33 11 100 100 183 S 19 53 42 58 42 32 42 N 17 18 29 6 94 88 184 N 19 5 53 74 47 11 53 N 18 61 11 6 6 6 185 Q 19 11 47 63 53 16 84 N 17 41 24 24 94 88 186 R 19 0 89 95 79 5 0 R 17 53 12 24 12 6 187 A 19 11 68 74 26 0 11 A 19 5 16 0 5 37 188 S 19 47 32 84 26 11 32 S 16 6 0 19 100 100 189 F 17 29 24 12 29 0 0 F 16 6 0 0 0 88 190 S 19 0 21 26 16 0 0 S 19 0 0 0 0 84 191 Q 19 5 5 11 11 0 0 Q 16 6 0 13 0 75 192 Y 19 0 32 53 26 0 5 Y 17 6 12 6 0 53 193 G 19 0 21 11 0 0 0 G 15 0 0 0 0 87 194 P 19 0 74 47 68 0 68 A 17 18 35 35 94 94 195 E 19 0 32 11 21 0 0 G 16 56 44 13 13 19 196 L 19 0 21 21 26 5 5 L 14 21 14 0 7 43 197 D 15 0 27 40 47 0 0 D 18 83 50 0 44 39 198 V 18 0 6 33 33 11 17 I 17 41 12 0 59 59 199 M 18 0 50 28 33 0 6 V 17 47 29 12 29 29 200 A 19 0 42 16 32 0 16 A 11 36 27 0 18 18 201 P 18 0 44 44 78 0 22 P 16 31 13 0 0 0 203 V 18 0 33 78 67 17 50 V 16 75 19 13 19 25 204 S 16 0 13 38 0 31 44 N 14 14 29 7 93 93 205 I 19 0 16 11 32 5 11 V 15 33 13 13 7 13 206 Q 19 68 53 32 84 26 16 Q 18 67 28 17 94 44 208 T 19 0 37 37 37 0 21 T 18 39 22 0 22 11 209 L 19 5 32 21 37 0 32 Y 18 83 67 0 89 44 210 P 19 0 74 42 68 0 11 P 17 100 100 29 94 24 211 G 19 5 79 79 53 21 37 G 15 53 67 20 93 93 212 N 19 26 42 42 32 5 16 S 13 46 46 38 92 92 213 K 17 47 94 100 18 94 29 T 18 22 39 6 94 94 214 Y 18 0 72 50 44 0 0 Y 18 100 39 0 22 17 215 G 19 11 68 26 32 11 0 A 17 71 59 41 100 94 216 A 19 42 32 42 37 53 21 S 18 56 72 33 100 100 217 Y 19 32 47 26 58 53 58 L 16 50 81 25 6 19 218 N 19 5 26 11 16 16 32 N 17 76 76 24 88 35 220 T 19 0 5 5 5 0 0 T 15 7 7 0 0 33 222 M 18 67 0 0 17 28 6 M 17 6 12 12 0 94 224 S 19 11 37 26 42 5 5 T 17 29 18 12 18 35 225 P 19 16 0 0 0 0 0 P 18 0 6 11 0 33 226 H 19 0 58 53 63 0 16 H 16 75 44 0 6 6 227 V 19 5 32 47 26 5 0 V 16 50 25 0 44 44 228 A 16 0 25 25 38 6 0 A 17 18 6 12 29 24 229 G 19 5 0 5 5 0 5 G 15 20 13 0 13 7 230 A 19 11 21 47 58 11 21 A 16 81 50 6 69 44 231 A 19 0 47 58 58 5 5 A 16 19 25 6 50 50 232 A 13 0 38 54 23 38 15 A 10 60 30 20 30 20 233 L 11 0 18 36 18 27 0 L 16 94 81 6 75 31 234 I 19 32 37 32 26 21 32 V 12 58 33 8 75 75 235 L 19 47 32 37 47 68 32 K 16 88 63 56 88 88 236 S 19 42 32 21 32 26 42 Q 16 94 88 13 75 50 237 K 19 79 26 37 26 37 58 K 17 94 71 65 88 82 238 H 19 0 37 47 42 58 26 N 17 71 71 47 94 88 239 P 19 0 58 16 47 84 53 P 17 71 82 65 100 82 240 N 19 42 68 11 47 79 42 S 14 71 93 14 93 79 241 W 19 0 68 21 79 63 58 W 19 42 63 63 95 84 242 T 19 32 16 74 32 89 21 S 15 33 33 47 100 73 243 N 19 11 11 63 37 21 16 N 18 39 50 39 94 89 244 T 19 47 16 74 53 68 37 V 16 56 75 63 94 81 245 Q 19 16 11 79 26 84 32 Q 13 62 77 46 100 77 246 V 17 6 18 35 18 18 12 I 17 76 24 29 35 35 247 R 19 0 53 74 42 0 0 R 19 53 68 21 84 79 248 S 19 47 37 79 42 32 58 N 16 69 56 31 94 88 249 S 19 42 5 68 37 5 42 H 18 17 28 39 94 83 250 L 19 0 26 32 26 0 16 L 17 65 12 0 29 24 251 E 19 0 37 11 63 0 0 K 14 64 50 50 86 64 252 N 19 21 58 37 74 53 42 N 16 38 81 63 88 75 253 T 19 16 53 58 68 11 16 T 14 36 29 7 93 79 254 T 19 16 53 47 63 11 5 A 18 39 22 0 22 11 255 T 19 26 58 53 37 0 42 T 17 18 29 35 94 94 256 K 19 11 89 95 58 0 68 S 17 47 82 35 100 65 257 L 19 0 47 53 32 0 16 L 15 87 40 0 40 13 258 G 17 0 47 82 94 0 0 G 17 82 59 0 82 53 259 D 19 21 5 0 11 0 89 S 12 83 100 8 100 25 260 S 19 26 63 63 37 0 47 T 14 64 86 21 100 79 261 F 19 0 0 32 11 5 0 N 16 56 88 63 100 75 262 Y 19 11 26 26 37 0 0 L 17 71 71 35 94 88 263 Y 19 5 37 32 26 0 5 Y 15 93 33 0 13 7 264 G 19 0 5 5 16 0 0 G 14 79 7 0 7 0 265 K 19 21 84 84 58 47 11 S 18 83 83 6 72 44 267 L 18 0 61 83 89 11 56 L 17 76 41 0 41 6 268 I 19 0 26 37 37 0 5 V 15 53 13 0 53 47 269 N 19 5 32 26 63 11 5 N 13 85 85 8 100 69 270 V 18 17 11 50 33 17 6 A 17 88 71 0 65 35 271 Q 19 53 32 32 79 47 26 E 14 29 100 0 100 64 272 A 19 26 16 68 32 37 16 A 16 69 63 25 100 69 273 A 13 0 69 85 100 0 0 A 15 100 73 7 73 27 274 A 19 5 42 0 53 16 26 T 15 87 80 13 87 60 275 Q 19 26 47 53 47 58 26 R 14 86 50 79 71 50

Restrictive sites are those having less than 20% neutral mutations for activity and stability. In Table 7-3 below, the results for variants that meet the definition of a restrictive site are shown as a percentage (%) of variants evaluated that meet definition of a neutral mutation (PI>0.5).

TABLE 7-3 Restrictive Sites for BPN′ and GG36 BPN′ BPN′ BPN′ GG36 BPN′ BMI BMI BMI GG36 BMI GG36 Position WT # BPN′ pH 7/ pH 8/ pH 8/ BPN′ BPN′ WT # GG36 pH 8/ GG36 LAS/ GG36 (BPN′ #) Residue Variants 16° C. 16° C. 32° LAS AAPF Residue Variants 32° C. Egg EDTA AAPF 23 G 18 11 17 11 11 6 G 13 15 15 15 15 32 D 16 0 0 0 0 0 D 17 12 18 0 0 64 H 13 0 0 0 0 0 H 14 0 0 7 0 65 G 17 6 12 12 6 6 G 10 0 0 0 0 70 G 16 0 0 0 0 0 G 12 0 0 0 0 83 G 19 5 5 5 5 5 G 10 10 10 0 10 125 S 19 16 5 5 5 0 S 15 13 7 13 0 168 P 19 16 11 0 0 0 P 18 6 6 0 0 202 G 19 0 0 11 0 0 G 18 6 0 0 0 221 S 16 0 0 0 0 0 S 16 0 0 0 0

In short as determined during development of the present invention, 10 positions in the mature region of two reference subtilisins are restrictive positions for activity and stability. Thus the remaining 265 positions in the mature region of two reference subtilisins are nonrestrictive positions (>20% neutral mutations) for activity and stability

Example 8 Protease Production in B. subtilis

In this Example, experiments conducted to produce various proteases in B. subtilis are described. In particular, the methods used in the transformation of B. subtilis with expression vectors for GG36, and BPN′-Y217L are provided. Transformation was performed as known in the art (See e.g., WO 02/14490).

GG36 Protease Production

In this Example, experiments conducted to produce GG36 (also referred to herein as B. lentos subtilisin) in B. subtilis are provided. The expression plasmid pAC-GG36ci was assembled using the GG36 codon-improved gene fused at the eighth codon of the aprE signal sequence under the control of the consensus aprE promoter and the BPN′ transcriptional terminator. In the sequence provided below, bold and italicized font indicates the consensus aprE promoter, standard font indicates the signal sequence, underlined font indicates the pro sequence, bold font indicates DNA that encodes the GG36 mature protease, and underlined italicized font indicates the BPN′ terminator. The coding region of the GG36 mature protease is flanked by KpnI and XhoI restriction sites for cloning purposes:

(SEQ ID NO: 560)

gtgagaagc aaaaaattgtggatcgtcgcgtcgaccgcattgctgatttctgttgct tttagctcatccatcgcatccgctgctgaagaagcaaaagaaaaatat ttaattggctttaatgagcaggaagctgtcagtgagtttgtagaacaa gttgaggcaaatgacgaggtagccattctctctgaggaagaggaagtc gaaattgaattgcttcatgaatttgaaacgattcctgttctgtccgtt gagttaagcccagaagatgtggacgcgttagagctcgatccagctatt tcttatattgaagaggatgcagaagtaactacaatg gcgcaatcggta ccatggggaattagcagagtacaagccccagctgcacataaccgtgga ttgacaggttctggtgtaaaagttgctgtccttgataccggtatttcc actcatccagacttaaatattcgtggtggagctagctttgtaccaggg gaaccatccactcaagatggcaatggacatggcactcatgttgccggc acaatcgcggctcttaacaattcaattggtgttcttggcgtagcgcca agcgcagaactatacgctgttaaagtattaggagcaagcggttcaggc tctgtcagctctattgcccaaggattggaatgggcagggaacaatggc atgcacgttgctaatcttagtttaggatctccttcgccaagtgccaca cttgagcaagctgttaatagcgcgacttctagaggcgttcttgttgta gcggcctctggaaattcaggtgcaggctcaatcagctatccggcccgt tatgcgaacgctatggcagtcggagctactgaccaaaacaacaaccgc gccagcttttcacagtatggcgcagggcttgacattgtcgcaccaggt gtaaacgtgcagagcacttacccaggttcaacatatgccagcttaaac ggtacatcaatggctactcctcatgttgcaggtgcggctgcacttgtt aaacaaaagaacccatcttggtccaatgtacaaatccgcaatcatctt aagaatacggcaactagcttaggaagcacaaacttgtatggaagcgga cttgtcaatgcagaagctgcaactcgttaa aagct taactcgagataa aaaaccggccttggccccgccggt tttttat

The amino acid sequence of the GG36 precursor protein is provided below. In this sequence, bold indicates the mature GG36 protease:

(SEQ ID NO: 561) MRSKKLWIVASTALLISVAFSSSIASAAEEAKEKYLIGFNEQEAVSEF VEQVEANDEVAILSEEEEVEIELLHEFETIPVLSVELSPEDVDALELD PAISYIEEDAEVTTMAQSVPWGISRVQAPAAHNRGLTGSGVKVAVLDT GISTHPDLNIRGGASFVPGEPSTQDGNGHGTHVAGTIAALNNSIGVLG VAPSAELYAVKVLGASGSGSVSSIAQGLEWAGNNGMHVANLSLGSPSP SATLEQAVNSATSRGVLVVAASGNSGAGSISYPARYANAMAVGATDQN NNRASFSQYGAGLDIVAPGVNVQSTYPGSTYASLNGTSMATPHVAGAA ALVKQKNPSWSNVQIRNHLKNTATSLGSTNLYGSGLVNAEAATR.

The amino acid sequence of the mature GG36 protease (SEQ ID NO:562) was used as the basis for making the variant libraries described herein:

(SEQ ID NO: 562) AQSVPWGISRVQAPAAHNRGLTGSGVKVAVLDTGISTHPDLNIRGGAS FVPGEPSTQDGNGHGTHVAGTIAALNNSIGVLGVAPSAELYAVKVLGA SGSGSVSSIAQGLEWAGNNGMHVANLSLGSPSPSATLEQAVNSATSRG VLVVAASGNSGAGSISYPARYANAMAVGATDQNNNRASFSQYGAGLDI VAPGVNVQSTYPGSTYASLNGTSMATPHVAGAAALVKQKNPSWSNVQI RNHLKNTATSLGSTNLYGSGLVNAEAATR.

Elements of plasmid pAC-GG36ci include: pUB110=DNA fragment from plasmid pUB110 (McKenzie et al., Plasmid 15:93-103 [1986]), pBR322=DNA fragment from plasmid pBR322 (Bolivar et al., Gene 2:95-113 [1977]), pC194=DNA fragment from plasmid pC194 (Horinouchi et al., J Bacteriol, 150:815-825 [1982]). The plasmid features as follows: On for B. subtilis=origin of replication from pUB110, CAT=chloramphenicol resistance gene from pC194, pMB1 origin=origin of replication from pBR322, bla=beta-lactamase from pBR322, Short aprE promoter=consensus transcriptional promoter, Signal Peptide=signal peptide, Pro Peptide=GG36 pro region, GG36ci Mature Peptide=mature GG36 (replaced by the coding regions for each variant expressed in this study), BPN′ Terminator=transcriptional terminator from subtilisin BPN′.

BPN′-Y217L (PURAFECT® PRIME Subtilisin) Protease Production

In this Example, experiments conducted to produce B. amyloliquefaciens subtilisin BPN′-Y217L (commercially available as PURAFECT® PRIME subtilisin; also referred to as “FNA”) in B. subtilis are described. The expression plasmid pAC-FNAre was assembled using the BPN′-Y217L gene, fused at the eighth codon of the aprE signal sequence under the control of the consensus aprE promoter and BPN′ transcriptional terminator. In the sequence provided below, bold and italicized font indicates the consensus aprE promoter, standard font indicates the signal sequence, underlined font indicates the pro sequence, bold font indicates DNA that encodes the BPN′-Y217L mature protease, and underlined italicized font indicates the BPN′ terminator. The coding region of the BPN′-Y217L mature protease contains the KvnI and XhoI restriction sites for cloning purposes:

(SEQ ID NO: 563)

gtgagaagcaaaaaattgtggatcagtttg ctgtttgctttagcgttaatctttacgatggcgttcggcagcacatcc agcgcgcaggctgcagggaaatcaaacggggaaaagaaatatattgtc gggtttaaacagacaatgagcacgatgagcgccgctaagaagaaagac gtcatttctgaaaaaggcgggaaagtgcaaaagcaattcaaatatgta gacgcagctagcgctacattaaacgaaaaagctgtaaaagaattgaaa aaagacccgagcgtcgcttacgttgaagaagatcacgtagcacacgcg tac gcgcagtccgtgccatatggcgtatcacaaattaaagcccctgct ctgcactctcaaggctacaccggttcaaatgttaaagtagcggttatc gacagcggtatcgattcttctcatccagatcttaaagtagcaggcgga gccagcatggttccttctgaaacaaatcctttccaagacaacaactct cacggaacacacgttgctggtaccgttgcggctcttaataactcaatc ggtgtattaggcgttgcgccaagcgcatcactttacgctgtaaaagtt ctcggcgccgacggttccggccaatacagctggatcattaacggaatc gagtgggcgatcgcaaacaatatggacgttattaacatgagcctcggc ggaccgtccggttctgctgctttaaaagcggcagttgataaagccgtt gcatccggcgtcgtagtcgttgcggcagccggcaacgaaggcacttcc ggcagctcaagcacagtgggctaccctggtaaatacccttctgtcatt gcagtaggcgctgtcgacagcagcaaccaaagagcatctttctcaagc gtaggacctgagctcgatgtcatggcacctggcgtatctatccaaagc acgcttcctggaaacaaatacggcgcgttgaacggtacatcaatggca tctccgcacgttgccggagccgcggctttgattctttctaagcacccg aactggacaaacactcaagtccgcagctctctagaaaacaccactaca aaacttggtgattctttctactatggaaaagggctgatcaatgtacag gcggcagctcagtaa aactcgagataaa aaaccggccttggccccgcc ggttttttat .

The amino acid sequence of the BPN′-Y217L precursor protein is provided below. In this sequence, bold indicates the mature BPN′-Y217L protease:

(SEQ ID NO: 564) MRSKKLWISLLFALALIFTMAFGSTSSAQAAGKSNGEKKYIVGFKQTM STMSAAKKKDVISEKGGKVQKQFKYVDAASATLNEKAVKELKKDPSVA YVEEDHVAHAYAQSVPYGVSQIKAPALHSQGYTGSNVKVAVIDSGIDS SHPDLKVAGGASMVPSETNPFQDNNSHGTHVAGTVAALNNSIGVLGVA PSASLYAVKVLGADGSGQYSWIINGIEWAIANNMDVINMSLGGPSGSA ALKAAVDKAVASGVVVVAAAGNEGTSGSSSTVGYPGKYPSVIAVGAVD SSNQRASFSSVGPELDVMAPGVSIQSTLPGNKYGALNGTSMASPHVAG AAALILSKHPNWTNTQVRSSLENTTTKLGDSFYYGKGLINVQAAAQ.

The amino acid sequence of the mature BPN′-Y217L protease was used as the basis for making the variant libraries described herein:

(SEQ ID NO: 565) AQSVPYGVSQIKAPALHSQGYTGSNVKVAVIDSGIDSSHPDLKVAGGA SMVPSETNPFQDNNSHGTHVAGTVAALNNSIGVLGVAPSASLYAVKVL GADGSGQYSWIINGIEWAIANNMDVINMSLGGPSGSAALKAAVDKAVA SGVVVVAAAGNEGTSGSSSTVGYPGKYPSVIAVGAVDSSNQRASESSV GPELDVMAPGVSIQSTLPGNKYGALNGTSMASPHVAGAAALILSKHPN WTNTQVRSSLENTTTKLGDSFYYGKGLINVQAAAQ.

Elements of plasmid pAC-FNAre include: pUB110=DNA fragment from plasmid pUB110 (McKenzie et al., Plasmid 15:93-103, [1986]), pBR322=DNA fragment from plasmid pBR322 (Bolivar et al., Gene 2:95-113 [1977]), pC194=DNA fragment from plasmid pC194 (Horinouchi et al., J. Bacteriol 150:815-825 [1982]). Plasmid features are as follows: On for B. subtilis=origin of replication from pUB110, CAT=chloramphenicol resistance gene from pC194, pMB1 origin=origin of replication from pBR322, bla=beta-lactamase from pBR322, Short aprE promoter=consensus transcriptional promoter, Signal Peptide=signal peptide, Pro Peptide=BPN′-Y217L pro region, BPN′-Y217L Mature Peptide=mature BPN′-Y217L (replaced by the coding regions for each variant expressed in this study), BPN′ Terminator=transcriptional terminator from subtilisin BPN′.

Example 9 Expression of Enzyme Variants

This Example describes the methods used to express various recombinant enzymes of transformed B. subtilis.

Subtilisins—2 ml scale

B. subtilis clones containing BPN′-Y217L or GG36 expression vectors were replicated with a steel 96-well replicator from glycerol stocks into 96-well culture plates (BD, 353075) containing 200 μl of LB media +25 μg/ml chloramphenicol, grown overnight at 37° C., 220 rpm in a humidified enclosure. A 200 μl aliquot from the overnight culture was used to inoculate 2000 μl defined media +25 μg/ml chloramphenicol in 5 ml plastic culture tubes. The cultivation media was an enriched semi-defined media based on MOPS buffer, with urea as major nitrogen source, glucose as the main carbon source, and supplemented with 1% soytone for robust cell growth. Culture tubes were incubated at 37° C., 220 rpm, for 60 hours. Following this incubation, the culture broths were centrifuged at greater than 8000×RCF. The supernatant solution was decanted into 15 ml polypropylene conical tubes for storage. No further purification or concentration was performed. Supernatant stocks were formulated to 40% propylene glycol final concentration for long-term stability and stored at 4° C.

Example 10 Production of Enzyme Variants

This Example describes the production of enzyme charge ladders and combinatorial charge libraries.

Enzyme Charge Ladders

Multiple protein variants spanning a range of physical properties of interest are selected from existing libraries or are generated by site-directed mutagenesis techniques as known in the art (See e.g., U.S. patent application Ser. Nos., 10/576,331, 11/581,102, and 11/583,334). This defined set of probe proteins is then assayed in a test of interest.

Exemplary protease charge ladder variants are shown in the following tables and assayed as described herein. In these tables, the charge change is relative to the wild-type enzyme.

TABLE 10-1 BPN′-Y217L Charge Ladder Variants BPN′-Y217L Variant (BPN′ numbering) Charge Change S87D-N109D-S188D-S248D −4 S87D-N109D-S188D −3 S87D-N109D −2 N109D −1 (BPN′-Y217L) 0 N109R +1 S87R-N109R +2 S87R-N109R-S188R +3 S87R-N109R-S188R-S248R +4

TABLE 10-2 GG36 Charge Ladder Variants GG36 Variant GG36 Variant Charge (GG36 numbering) (BPN′ numbering) Change S85D-Q107D-S182D-N242D S87D-Q109D-S188D-N248D −4 S85D-Q107D-S182D S87D-Q109D-S188D −3 S85D-Q107D S87D-Q109D −2 Q107D Q109D −1 (GG36) (GG36) 0 Q107R Q109R +1 S85R-Q107R S87R-Q109R +2 S85R-Q107R-S182R S87R-Q109R-S188R +3 S85R-Q107R-S182R-N242R S87R-Q109R-S188R-N248R +4

Enzyme Combinatorial Charge Libraries

Generation of B. lentus Subtilisin (=GG36) Combinatorial Charge Libraries

The pAC-GG36ci plasmid containing the codon-improved GG36 gene was sent to DNA 2.0, for the generation of combinatorial charge libraries (CCL). They were also provided with the Bacillus subtilis strain (genotype: ΔaprE, ΔnprE, ΔspoIIE, amyE::xylRPxylAcomK-phleo) for transformations. In addition a request was made to DNA2.0 Inc. for the generation of positional libraries at each of the four sites in GG36 protease that are shown in Table 10-3. Variants were supplied as glycerol stocks in 96-well plates.

The GG36 CCL was designed by identifying four well-distributed, surface-exposed, uncharged polar amino-acid residues outside the active site. These residues are Ser-85, Gln-107, Ser-182, and Asn-242 (residues 87, 109, 188, and 248 in BPN′ numbering). An 81-member combinatorial library (G-1 to G-81) was created by making all combinations of three possibilities at each site: wild-type, arginine, or aspartic acid.

TABLE 10-3 GG36 CCL Variants Charge Variant # S 85 Q 107 S 182 N 242 Change G-01 — — — — 0 G-02 — — — D −1 G-03 — — — R +1 G-04 — — D — −1 G-05 — — D D −2 G-06 — — D R 0 G-07 — — R — +1 G-08 — — R D 0 G-09 — — R R +2 G-10 — D — — −1 G-11 — D — D −2 G-12 — D — R 0 G-13 — D D — −2 G-14 — D D D −3 G-15 — D D R −1 G-16 — D R — 0 G-17 — D R D −1 G-18 — D R R +1 G-19 — R — — +1 G-20 — R — D 0 G-21 — R — R +2 G-22 — R D — 0 G-23 — R D D −1 G-24 — R D R +1 G-25 — R R — +2 G-26 — R R D +1 G-27 — R R R +3 G-28 D — — — −1 G-29 D — — D −2 G-30 D — — R 0 G-31 D — D — −2 G-32 D — D D −3 G-33 D — D R −1 G-34 D — R — 0 G-35 D — R D −1 G-36 D — R R +1 G-37 D D — — −2 G-38 D D — D −3 G-39 D D — R −1 G-40 D D D — −3 G-41 D D D D −4 G-42 D D D R −2 G-43 D D R — −1 G-44 D D R D −2 G-45 D D R R 0 G-46 D R — — 0 G-47 D R — D −1 G-48 D R — R +1 G-49 D R D — −1 G-50 D R D D −2 G-51 D R D R 0 G-52 D R R — +1 G-53 D R R D 0 G-54 D R R R +2 G-55 R — — — +1 G-56 R — — D 0 G-57 R — — R +2 G-58 R — D — 0 G-59 R — D D −1 G-60 R — D R +1 G-61 R — R — +2 G-62 R — R D +1 G-63 R — R R +3 G-64 R D — — 0 G-65 R D — D −1 G-66 R D — R +1 G-67 R D D — −1 G-68 R D D D −2 G-69 R D D R 0 G-70 R D R — +1 G-71 R D R D 0 G-72 R D R R +2 G-73 R R — — +2 G-74 R R — D +1 G-75 R R — R +3 G-76 R R D — +1 G-77 R R D D 0 G-78 R R D R +2 G-79 R R R — +3 G-80 R R R D +2 G-81 R R R R +4 Generation of B. amyloliquefaciens Subtilisin BPN′-Y217L CCL

The pAC-FNAre plasmid containing the BPN′-Y217L gene was sent to DNA 2.0 Inc. (Menlo Park, Calif.) for the generation of CCL. They were also provided with the Bacillus subtilis strain (genotype: ΔaprE, ΔnprE, ΔspoIIE, amyE::xylRPxylAcomK-phleo) for transformations. A request was made to DNA 2.0 Inc. for the generation of positional libraries at each of the four BPN′-Y217L protease sites that are shown in Table 10-4. Variants were supplied as glycerol stocks in 96-well plates.

The subtilisin BPN′-Y217L combinatorial charge library was designed by identifying four well-distributed, surface-exposed, uncharged polar amino-acid residues outside the active site. These residues are Ser-87, Asn-109, Ser-188, and Ser-248. An 81-member combinatorial library (F-1 to F-81) was created by making all combinations of three possibilities at each site: wild-type, arginine, or aspartic acid.

TABLE 10-4 BPN′-Y217L CCL Variants Charge Variant # S 87 N 109 S 188 S 248 Change F-01 — — — — 0 F-02 — — — D −1 F-03 — — — R +1 F-04 — — D — −1 F-05 — — D D −2 F-06 — — D R 0 F-07 — — R — +1 F-08 — — R D 0 F-09 — — R R +2 F-10 — D — — −1 F-11 — D — D −2 F-12 — D — R 0 F-13 — D D — −2 F-14 — D D D −3 F-15 — D D R −1 F-16 — D R — 0 F-17 — D R D −1 F-18 — D R R +1 F-19 — R — — +1 F-20 — R — D 0 F-21 — R — R +2 F-22 — R D — 0 F-23 — R D D −1 F-24 — R D R +1 F-25 — R R — +2 F-26 — R R D +1 F-27 — R R R +3 F-28 D — — — −1 F-29 D — — D −2 F-30 D — — R 0 F-31 D — D — −2 F-32 D — D D −3 F-33 D — D R −1 F-34 D — R — 0 F-35 D — R D −1 F-36 D — R R +1 F-37 D D — — −2 F-38 D D — D −3 F-39 D D — R −1 F-40 D D D — −3 F-41 D D D D −4 F-42 D D D R −2 F-43 D D R — −1 F-44 D D R D −2 F-45 D D R R 0 F-46 D R — — 0 F-47 D R — D −1 F-48 D R — R +1 F-49 D R D — −1 F-50 D R D D −2 F-51 D R D R 0 F-52 D R R — +1 F-53 D R R D 0 F-54 D R R R +2 F-55 R — — — +1 F-56 R — — D 0 F-57 R — — R +2 F-58 R — D — 0 F-59 R — D D −1 F-60 R — D R +1 F-61 R — R — +2 F-62 R — R D +1 F-63 R — R R +3 F-64 R D — — 0 F-65 R D — D −1 F-66 R D — R +1 F-67 R D D — −1 F-68 R D D D −2 F-69 R D D R 0 F-70 R D R — +1 F-71 R D R D 0 F-72 R D R R +2 F-73 R R — — +2 F-74 R R — D +1 F-75 R R — R +3 F-76 R R D — +1 F-77 R R D D 0 F-78 R R D R +2 F-79 R R R — +3 F-80 R R R D +2 F-81 R R R R +4

Example 11 Variant BPN′-Y217L and GG36 Subtilisin Performance

This Example describes the testing of BPN′-Y217L and GG36 variants in BMI microswatch and baked egg assays in detergents representing various market geographies (e.g., differing pH, T, and/or water hardness), in both laundry and automatic dishwashing applications, as described in Example 1.

The above observations hold for other serine proteases such as the subtilisins BPN′-Y217L and GG36. For instance FIGS. 2A and 2B shows an optimum charge for BPN′-Y217L and GG36 respectively, in cleaning performance under North American laundry conditions using off-the-shelf, heat-inactivated TIDE® 2× detergent. The left Y-axes shows microswatch cleaning performance, where a higher number indicates superior BMI stain removal. The right Y-axes shows the performance index defined as cleaning performance of variants (filled symbols) relative to the parent molecule (unfilled symbols). The horizontal lines indicate a performance index at either 2 or 3 standard deviations above the noise of the assay. The BPN′-Y217L charge combinatorial library (CCL) exhibits a charge optimum at zero charge changes with respect to the parent BPN′-Y217L while the GG36 CCL exhibits an optimum at negative two charges relative to the GG36 parent.

FIGS. 3A, 3B, 4A, 4B, 5A and 5B demonstrate that the location of the charge optimum is a function of the solution environment determined by detergent formulation, pH, temperature and ionic strength due to water hardness and detergent concentration. For instance the charge optimum for BPN′-Y217L CCL shifts dramatically from zero under North American laundry conditions to more positive charges under Western European and Japanese conditions. Moreover the charge optimum is observed for both liquid and granular (powder) laundry detergent formulations. Similarly, a charge optimum was observed for both BPN′-Y217L and GG36 CCL in automatic dish washing (ADW) detergent against (e.g., Reckitt Benckiser Calgonit 40° C., 12 gpg, pH 10) baked egg as the enzyme substrate.

As demonstrated during development of the present invention, the cleaning performance of protease charge variants (e.g., GG36, BPN′-Y217L, etc) in different detergents is largely dominated by the working solution pH and conductivity. Final conductivity is a measure of ionic strength and is due to water hardness, detergent concentration and composition. For instance, there is a correlation between cleaning performance of GG36 and BPN′-Y217L variants against baked egg stains under European and North American ADW detergent when carried out at pH 10.6 and conductivity of 3.0 mS/cm. In particular, cleaning performance of charge variants is well correlated provided pH and conductivity are the same. This finding makes it possible to screen enzyme performance using a given detergent, for extrapolation of those results to another detergent of matching pH and conductivity. Likewise it is possible to screen enzyme performance in a buffer of matching pH and conductivity, for extrapolation of those results to a detergent exhibiting similar working pH and conductivity.

TABLE 11-1 Net PI NA PI WE PI Dish Variants Charge Laundry Laundry baked egg GG36 0 1.000 1.000 1.000 G-2 −1 0.950 0.939 1.450 G-3 1 0.578 0.759 1.231 G-4 −1 1.219 1.539 1.467 G-5 −2 1.261 1.194 1.508 G-6 0 0.936 0.999 1.563 G-7 1 0.568 0.834 0.712 G-8 0 0.043 0.151 −0.033 G-9 2 0.350 0.601 0.708 G-10 −1 1.266 1.089 1.022 G-11 −2 1.280 1.209 0.788 G-12 0 0.810 1.074 0.977 G-13 −2 1.317 1.411 1.300 G-14 −3 0.080 0.144 −0.007 G-15 −1 0.917 1.254 1.393 G-16 0 0.750 1.081 0.742 G-17 −1 0.815 0.894 0.909 G-18 1 0.675 0.931 0.867 G-19 1 0.713 0.856 1.310 G-20 0 0.071 0.129 −0.015 G-21 2 0.434 0.834 1.098 G-22 0 0.782 1.014 1.447 G-23 −1 0.964 0.939 1.396 G-24 1 0.466 0.729 1.368 G-25 2 0.322 0.744 0.638 G-26 1 0.517 0.984 0.694 G-27 3 0.303 1.074 0.971 G-28 −1 1.126 1.141 1.023 G-29 −2 1.126 0.991 1.037 G-30 0 0.945 1.149 1.006 G-31 −2 1.331 1.149 1.412 G-32 −3 1.345 0.999 1.303 G-33 −1 0.950 1.036 1.420 G-34 0 0.671 0.999 0.673 G-35 −1 0.694 1.021 1.026 G-36 1 0.415 0.774 0.704 G-37 −2 1.410 1.554 −0.011 G-38 −3 0.457 0.759 1.081 G-39 −1 0.936 1.186 0.940 G-40 −3 0.043 0.106 −0.006 G-41 −4 1.163 0.496 0.988 G-42 −2 1.359 1.276 1.165 G-43 −1 0.782 1.119 0.740 G-44 −2 0.926 1.051 0.748 G-45 0 0.503 0.961 0.619 G-46 0 0.759 0.916 1.035 G-47 −1 0.871 1.051 1.057 G-48 1 0.452 0.864 1.060 G-49 −1 0.885 0.909 1.239 G-50 −2 0.912 0.909 1.613 G-51 0 0.638 1.006 1.723 G-52 1 0.396 0.909 0.820 G-53 0 0.568 0.909 0.806 G-54 2 0.345 0.766 0.641 G-55 1 0.689 1.036 1.230 G-56 0 0.675 1.134 0.818 G-57 2 0.452 0.766 0.922 G-58 0 1.024 1.216 1.444 G-59 −1 1.131 1.306 1.473 G-60 1 0.699 0.946 1.520 G-61 2 0.457 0.886 0.680 G-62 1 0.759 1.059 1.169 G-63 3 0.327 0.669 0.687 G-64 0 0.847 1.119 1.001 G-65 −1 0.601 0.879 1.014 G-66 1 1.001 1.261 1.042 G-67 −1 1.196 1.411 1.489 G-68 −2 1.131 1.179 1.163 G-69 0 0.768 0.999 1.488 G-70 1 0.647 1.809 0.229 G-71 0 0.620 1.081 0.631 G-72 2 0.364 0.819 0.634 G-73 2 0.387 0.729 0.997 G-74 1 0.638 0.939 1.105 G-75 3 0.657 0.856 1.081 G-76 1 0.071 0.136 −0.018 G-77 0 0.866 0.969 1.400 G-78 2 0.434 0.789 1.175 G-79 3 0.327 0.789 0.874 G-80 2 0.355 0.781 0.833 G-81 4 0.229 0.466 0.653

TABLE 11-2 Net PI NA PI WE PI JPN PI dish Variants Charge Laundry Laundry Laundry baked egg BPN′-Y217L 0 1.000 1.000 1.000 1.000 F-2 −1 0.828 0.794 1.020 1.572 F-3 1 0.866 1.687 1.712 1.322 F-4 −1 0.814 0.868 0.810 1.211 F-5 −2 0.753 0.988 0.458 1.395 F-6 0 1.032 1.479 1.529 1.273 F-7 1 0.805 1.792 1.359 0.969 F-8 0 0.909 1.360 1.576 0.855 F-9 2 0.705 1.360 1.529 0.777 F-10 −1 1.102 0.749 0.607 1.073 F-11 −2 0.904 0.600 0.410 1.004 F-12 0 1.221 1.911 1.583 1.030 F-13 −2 0.838 0.690 0.234 0.832 F-14 −3 0.549 0.705 0.139 0.665 F-15 −1 1.093 1.107 0.654 1.063 F-16 0 1.268 1.524 1.258 0.571 F-17 −1 0.819 0.764 0.722 0.710 F-18 1 1.098 1.226 1.705 0.742 F-19 1 1.003 1.196 1.590 1.298 F-20 0 0.875 1.047 1.542 1.328 F-21 2 0.866 1.568 1.976 1.327 F-22 0 1.017 1.211 1.569 1.736 F-23 −1 0.771 1.241 0.973 1.335 F-24 1 0.970 2.045 1.942 1.668 F-25 2 0.738 1.315 1.664 1.015 F-26 1 0.937 1.434 1.624 0.919 F-27 3 0.535 1.122 1.990 1.283 F-28 −1 0.743 0.854 0.776 0.946 F-29 −2 0.691 0.749 0.451 0.707 F-30 0 1.183 1.464 1.549 0.979 F-31 −2 0.738 0.720 0.519 1.185 F-32 −3 0.497 0.645 0.376 0.908 F-33 −1 1.107 1.062 1.332 0.989 F-34 0 0.809 1.241 1.393 0.640 F-35 −1 0.672 0.824 0.844 0.928 F-36 1 0.823 1.211 1.420 1.130 F-37 −2 0.880 0.720 0.227 0.678 F-38 −3 0.597 0.779 0.139 0.865 F-39 −1 0.890 1.017 0.661 0.760 F-40 −3 0.469 0.660 0.132 0.568 F-41 −4 0.322 0.541 0.064 0.464 F-42 −2 1.022 0.720 0.247 0.948 F-43 −1 0.852 1.092 0.980 0.605 F-44 −2 0.530 0.794 0.369 0.804 F-45 0 0.980 1.419 1.122 0.730 F-46 0 0.819 1.002 1.380 0.999 F-47 −1 0.984 0.928 1.102 1.172 F-48 1 0.956 1.419 2.010 1.377 F-49 −1 0.913 0.898 0.925 1.263 F-50 −2 0.743 0.779 0.756 1.084 F-51 0 1.008 1.300 1.481 1.588 F-52 1 0.800 1.360 1.481 0.851 F-53 0 0.705 1.077 1.271 0.792 F-54 2 0.677 1.270 1.468 1.172 F-55 1 1.050 1.538 1.515 0.996 F-56 0 1.112 1.122 1.088 0.721 F-57 2 0.866 1.330 2.173 1.014 F-58 0 1.036 1.107 1.183 1.341 F-59 −1 1.117 1.077 0.898 0.878 F-60 1 0.928 1.449 1.976 1.483 F-61 2 0.942 1.687 1.542 0.785 F-62 1 1.017 1.494 1.651 1.010 F-63 3 0.630 1.613 1.522 0.910 F-64 0 1.131 1.241 0.912 0.907 F-65 −1 0.994 0.958 1.136 0.582 F-66 1 1.216 1.464 2.308 0.985 F-67 −1 1.126 0.854 0.485 0.855 F-68 −2 0.748 0.705 0.261 0.794 F-69 0 1.249 1.479 1.041 0.925 F-70 1 1.050 1.911 1.631 0.878 F-71 0 1.136 1.687 1.298 0.998 F-72 2 0.871 2.893 1.949 0.850 F-73 2 0.998 1.717 1.990 1.276 F-74 1 1.102 1.509 2.281 1.186 F-75 3 0.672 1.687 2.044 1.351 F-76 1 0.946 1.449 1.807 1.647 F-77 0 1.050 1.509 1.793 1.287 F-78 2 0.975 1.256 2.207 1.786 F-79 3 0.606 1.285 1.508 0.954 F-80 2 0.795 2.655 1.800 0.896 F-81 4 0.611 1.419 1.759 0.965

Example 12 LAS and Chelant Stability

This Example describes determining the relationship between protein charge and stability in a reaction medium containing one or both of an anionic surfactant and a chelant. For the determination of protease activity of the stressed and unstressed samples, the suc-AAPF-pNA assay was used. For determination of the alpha-amylase activity of the stressed and unstressed samples, the BODIPY-starch assay was used. Residual LAS and EDTA from the stress plates do not affect the suc-AAPF-pNA or BODIPY-starch assays.

LAS/EDTA Stability

Reagents used included: control buffer: 50 mM HEPES, 0.005% Tween-80, pH 8.0; and stress buffer 50 mM HEPES, 0.1% (w/v) LAS (dodecylbenzene-sulfonate, sodium salt, Sigma D-2525), 10 mM EDTA, pH 8.0. Enzyme variants (20 ppm) were diluted 1:20 into 96-well non-binding flat-bottom plate containing either control or stress buffer and mixed. The control plate was incubated at room temperature while the stress plate was immediately placed at 37° C. for 30-60 min (depending on the stability of the enzyme being tested). Following incubation, enzyme activity was measured using suc-AAPF-pNA assay for proteases. The fraction of remaining or residual activity was equal to the reaction rate of the stressed sample divided by the reaction rate of the control sample. The parent enzymes and variants were found to be stable for 60 min in the control buffer.

FIG. 6 depicts LAS/EDTA stability as a function of net charge change relative to parent BPN′-Y217L, for a library containing 80 variants. This library was designed and constructed according to the methods described in Example 2, to span several net charges relative to the parent BPN′-Y217L molecule. As evidenced from the Figure, accumulation of negative charges (up to −4) relative to parent BPN′-Y217L, are beneficial for combined LAS/chelant stability. This is an example of optimizing a protein physical property, in this case net charge, for improving protein stability in a complex liquid laundry environment.

Example 13 Stain Removal Performance of BPN′ Multiple Mutation Library (MML) Variants

BPN′ multiple mutation libraries (or combinatorial libraries) were produced by Geneart or DNA 2.0, as described previously herein, using BPN′ as the parent protein. The BPN′ variant proteins were also produced as described earlier. Protein concentration of culture supernatants was determined by TCA precipitation as described in Example 1. The stain removal performance of the variants was tested in laundry applications on EMPA 116 swatches (BMI stain, CFT) at pH 8/16° C., pH 7/16° C. and pH 8/32° C. using methods described in Example 1, with the following modifications. The test detergent used was heat inactivated TIDE® 2× Cold detergent (Procter & Gamble). Heat inactivation of commercial detergent formulas serves to destroy the endogenous enzymatic activity of any protein components while retaining the properties of nonenzymatic components. Heat inactivation of the detergents was performed by placing pre-weighed amounts of liquid detergent (in a glass bottle) in a water bath at 95° C. for 2 hours. The detergent was purchased from local supermarket stores. Both unheated and heated detergents were assayed within 5 minutes of dissolving the detergent, in order to accurately determine percentage deactivated. Enzyme activity was tested by AAPF assay. Functionality of BPN′ variants was quantified as a performance index (Pi) (i.e., the ratio of performance of a variant relative to parent BPN′). Results are shown in Table 13-1. BPN′ variants showing a Pi value greater than or equal to 0.5 for one or more BMI stain removal performance tests and/or TCA precipitation showed improved cleaning benefits and/or expression. Performance indices less than or equal to 0.05 were fixed to 0.05 and indicated in bold italics in the table. For every variant with a TCA protein performance index less than or equal to 0.05, all values were fixed at 0.05. In this Table, “ND” indicates “not determined”

TABLE 13-1 P_(i) Values of BPN′ Variants Tested for Expression (TCA) and Stain Removal Performance (BMI pH 8/16° C., BMI pH 7/16° C., and BMI pH 8/32° C.) BMI BMI BMI Variant Code TCA pH 8/16° C. pH 7/16° C. pH 8/32° C. Parent BPN′ 1.00 1.00 1.00 1.00 BPN′Y217L 1.01 1.12 1.08 1.08 A92G 0.52 1.04 ND ND A92G-G100T 0.58 0.37 ND ND A92G-G128A 0.49 0.83 ND ND A92G-G97A 0.77 1.14 ND ND A92G-I111V 0.6 1.02 ND ND A92G-L126A 0.68 1.14 ND ND A92G-L96T 0.68 0.69 ND ND A92G-M124V 0.55 1.07 ND ND A92G-N123G 0.46 0.42 ND ND A92G-V227T 0.52 0.54 ND ND A92G-W106F 0.44 0.4 ND ND A92G-Y104N 0.65 0.41 ND ND A92G-Y167A 0.44 0.56 ND ND A92G-Y217Q 0.56 1.2 ND ND BPN′-Y217L 1.01 1.12 1.08 1.08 G100T 0.71 1.14 ND ND G100T-G128A 0.46 0.14 ND ND G100T-I111V 0.46 0.77 ND ND G100T-L126A 0.59 0.1 ND ND G100T-M124V 0.57 0.05 ND ND G100T-N123G 0.56 0.05 ND ND G100T-V227T 0.37 0.42 ND ND G100T-W106F 0.62 0.05 ND ND G100T-Y104N 0.68 0.05 ND ND G100T-Y167A 0.63 0.28 ND ND G100T-Y217Q 0.7 1.11 ND ND G128A 1.5 1.17 1.11 1.14 G128A-V227T 0.48 0.86 ND ND G128A-Y167A 0.57 0.78 ND ND G128A-Y217Q 1.19 1.38 1.12 1.16 G97A 1.37 1.12 1.03 1.1  G97A-G100T 0.6 0.99 ND ND G97A-G128A 1.17 1.19 1.06 1.02 G97A-I111V 1 1.22 ND ND G97A-L126A 1.36 1.24 1.1  1.11 G97A-M124V 1.33 1.29 1.12 1.12 G97A-N123G 0.91 1.22 1.19 1.12 G97A-V227T 0.71 1.07 ND ND G97A-W106F 0.69 1.1 ND ND G97A-Y104N 0.69 1.1 ND ND G97A-Y167A 0.66 1.02 ND ND G97A-Y217Q 1.42 1.27 1.08 1.14 I111V 1.07 1.04 ND ND I111V-G128A 1.13 1.1 ND ND I111V-L126A 1.09 1.07 ND ND I111V-M124V 0.93 1.3 ND ND I111V-N123G 0.67 1.09 ND ND I111V-V227T 0.56 1.01 ND ND I111V-Y167A 0.66 0.97 ND ND I111V-Y217Q 1.06 1.28 ND ND L126A 1.56 1.16 1.1  1.08 L126A-G128A 0.76 0.83 0.9  0.92 L126A-V227T 0.73 0.8 ND ND L126A-Y167A 0.73 0.76 ND ND L126A-Y217Q 1.7 1.28 1.11 1.11 L96T 0.84 1.17 1.04 1.13 L96T-G100T 0.53 0.14 ND ND L96T-G128A 0.59 0.77 0.77 0.84 L96T-G97A 0.81 1.24 1.11 1.14 L96T-I111V 0.49 0.94 ND ND L96T-L126A 0.76 0.43 0.37 0.6  L96T-M124V 0.87 1.12 0.93 1.01 L96T-N123G 0.58 0.3 0.22 0.56 L96T-V227T 0.5 0.3 ND ND L96T-W106F 0.57 0.41 ND ND L96T-Y104N 0.43 0.05 ND ND L96T-Y167A 0.36 0.63 ND ND L96T-Y217Q 0.79 1.28 1   1.12 M124V 1.61 1.22 1.12 1.15 M124V-G128A 0.96 1.17 1.11 1.12 M124V-L126A 1.74 1.13 1.12 1.11 M124V-V227T 0.65 0.96 ND ND M124V-Y167A 0.56 1.17 ND ND M124V-Y217Q 1.47 1.37 1.09 1.19 N123G 1 1.16 1.12 1.03 N123G-G128A 0.5 0.75 0.88 0.85 N123G-L126A 0.72 0.62 0.48 0.65 N123G-M124V 0.59 0.6 0.54 0.66 N123G-V227T 0.65 0.05 ND ND N123G-Y167A 0.59 0.34 ND ND N123G-Y217Q 0.82 1.25 1.18 1.13 N62Q 1.63 1.29 1.19 1.06 N62Q-A92G 0.59 1.17 ND ND N62Q-G100T 0.57 0.96 ND ND N62Q-G128A 1.09 1.21 1.15 1.12 N62Q-G97A 1.52 1.32 1.22 1.17 N62Q-I111V 1.4 1.25 ND ND N62Q-L126A 1.46 1.07 0.99 1.03 N62Q-L96T 0.73 1.02 0.97 0.99 N62Q-M124V 1.29 1.23 1.06 1.15 N62Q-N123G 0.57 1.06 0.97 1   N62Q-S89Y 0.6 1.17 ND ND N62Q-V227T 0.57 1.06 ND ND N62Q-V68A 1.86 1.08 ND ND N62Q-Y104N 0.59 0.66 ND ND N62Q-Y167A 0.79 1.15 ND ND N62Q-Y217Q 1.35 1.28 1.13 1.21 P52L 0.5 0.59 ND ND P52L-A92G 0.69 0.2 ND ND P52L-G100T 0.59 0.39 ND ND P52L-G128A 0.55 0.51 ND ND P52L-G97A 0.54 0.78 ND ND P52L-I111V 0.43 0.68 ND ND P52L-L126A 0.69 0.6 ND ND P52L-L96T 0.67 0.34 ND ND P52L-M124V 0.56 0.72 ND ND P52L-N123G 0.48 0.34 ND ND P52L-N62Q 0.54 0.77 ND ND P52L-S89Y 0.51 0.42 ND ND P52L-V227T 0.38 0.27 ND ND P52L-V68A 0.6 1.2 ND ND P52L-W106F 0.43 0.52 ND ND P52L-Y104N 0.64 0.32 ND ND P52L-Y167A 0.38 0.4 ND ND P52L-Y217Q 0.34 0.77 ND ND S89Y 0.94 1.07 ND ND S89Y-A92G 0.5 0.9 ND ND S89Y-G100T 0.65 0.67 ND ND S89Y-G128A 0.98 1.1 ND ND S89Y-G97A 1.26 1.06 ND ND S89Y-I111V 0.83 1.07 ND ND S89Y-L126A 0.93 1.17 ND ND S89Y-L96T 0.77 0.84 ND ND S89Y-M124V 1.1 1.31 ND ND S89Y-N123G 0.47 0.85 ND ND S89Y-V227T 0.66 0.87 ND ND S89Y-W106F 0.7 0.98 ND ND S89Y-Y104N 0.74 0.64 ND ND S89Y-Y167A 0.55 0.91 ND ND S89Y-Y217Q 1.32 1.17 ND ND V227T 0.65 1.09 ND ND V68A 2.02 1.33 ND ND V68A-A92G 0.81 1.42 ND ND V68A-G100T 0.87 0.31 ND ND V68A-G128A 1.16 1.28 ND ND V68A-G97A 2.12 1.33 ND ND V68A-I111V 2.06 1.31 ND ND V68A-L126A 1.66 0.58 ND ND V68A-L96T 0.68 0.86 ND ND V68A-M124V 1.25 0.96 ND ND V68A-N123G 0.92 0.69 ND ND V68A-S89Y 1.65 1.37 ND ND V68A-V227T 1 1.35 ND ND V68A-W106F 0.7 1.29 ND ND V68A-Y104N 0.71 0.78 ND ND V68A-Y167A 0.87 1.19 ND ND V68A-Y217Q 2.34 1.32 ND ND W106F 0.78 1.17 ND ND W106F-G128A 0.68 0.86 ND ND W106F-I111V 0.61 1.06 ND ND W106F-L126A 0.67 0.82 ND ND W106F-M124V 0.56 0.96 ND ND W106F-N123G 0.47 0.29 ND ND W106F-V227T 0.45 0.76 ND ND W106F-Y167A 0.75 0.66 ND ND W106F-Y217Q 0.87 1.35 ND ND Y104N 0.88 1.03 ND ND Y104N-G128A 0.83 1.21 ND ND Y104N-I111V 0.6 0.94 ND ND Y104N-L126A 0.59 0.17 ND ND Y104N-M124V 0.51 0.43 ND ND Y104N-N123G 0.58 0.21 ND ND Y104N-V227T 0.4 0.32 ND ND Y104N-W106F 0.52 0.46 ND ND Y104N-Y167A 0.74 0.51 ND ND Y104N-Y217Q 0.68 1.27 ND ND Y167A 0.77 0.89 ND ND Y167A-V227T 0.45 0.43 ND ND Y167A-Y217Q 0.64 1.21 ND ND Y217Q 1.37 1.26 ND ND Y217Q-V227T 0.87 1.08 ND ND

Example 14 Stain Removal Performance of BPN′ Two Site Variants

Using BPN′ as the parent protein, two site variants were generated at positions 217 and 222 (BPN′ numbering) using fusion PCR. The BPN′ variant proteins were produced as described before. Protein concentration of culture supernatants was determined by TCA precipitation as described in Example 1. The stain removal performance of the variants was tested in laundry applications on EMPA 116 swatches (BMI stain, CFT) at pH 8/16° C. in heat-inactivated TIDE® 2× Cold (Procter & Gamble) using methods described in Example 1. Functionality of BPN′ variants was quantified as a performance index (Pi) (i.e., the ratio of performance of a variant relative to BPN′-Y217L. Results are shown in Table 14-1. BPN′ variants showing a Pi value greater than or equal to 0.5 for the BMI stain removal performance tests and/or TCA precipitation showed improved cleaning benefits and/or expression.

TABLE 14-1 Stain Removal Performance and Expression of BPN′ Two Site Variants Variant BMI TCA Y217L-M222Q 0.88 1.27 Y217Q-M222Q 1.08 1.18 Y217V-M222Q 1.02 0.76

Example 15 ASP Protease Production in B. subtilis

Experiments conducted to produce 69B4 protease (also referred to herein as “ASP,” “Asp,” and “ASP protease,” and “Asp protease”) in B. subtilis are described in U.S. patent application Ser. No. 10/576,331, incorporated herein by reference in its entirety. Briefly, the DNA sequence (synthetic ASP DNA sequence) provided below, with codon usage adapted for Bacillus species, encodes the wild type ASP precursor protein:

(SEQ ID NO: 566) ATGACACCACGAACTGTCACAAGAGCTCTGGCTGTGGCAACAGCAGCT GCTACACTCTTGGCTGGGGGTATGGCAGCACAAGCTAACGAACCGGCT CCTCCAGGATCTGCATCAGCCCCTCCACGATTAGCTGAAAAACTTGAC CCTGACTTACTTGAAGCAATGGAACGCGATCTGGGGTTAGATGCAGAG GAAGCAGCTGCAACGTTAGCTTTTCAGCATGACGCAGCTGAAACGGGA GAGGCTCTTGCTGAGGAACTCGACGAAGATTTCGCGGGCACGTGGGTT GAAGATGATGTGCTGTATGTTGCAACCACTGATGAAGATGCTGTTGAA GAAGTCGAAGGCGAAGGAGCAACTGCTGTGACTGTTGAGCATTCTCTT GCTGATTTAGAGGCGTGGAAGACGGTTTTGGATGCTGCGCTGGAGGGT CATGATGATGTGCCTACGTGGTACGTCGACGTGCCTACGAATTCGGTA GTCGTTGCTGTAAAGGCAGGAGCGCAGGATGTAGCTGCAGGACTTGTG GAAGGCGCTGATGTGCCATCAGATGCGGTCACTTTTGTAGAAACGGAC GAAACGCCTAGAACGATG TTCGACGTAATTGGAGGCAACGCATATACT ATTGGCGGCCGGTCTAGATGTTCTATCGGATTCGCAGTAAACGGTGGC TTCATTACTGCCGGTCACTGCGGAAGAACAGGAGCCACTACTGCCAAT CCGACTGGCACATTTGCAGGTAGCTCGTTTCCGGGAAATGATTATGCA TTCGTCCGAACAGGGGCAGGAGTAAATTTGCTTGCCCAAGTCAATAAC TACTCGGGCGGCAGAGTCCAAGTAGCAGGACATACGGCCGCACCAGTT GGATCTGCTGTATGCCGCTCAGGTAGCACTACAGGTTGGCATTGCGGA ACTATCACGGCGCTGAATTCGTCTGTCACGTATCCAGAGGGAACAGTC CGAGGACTTATCCGCACGACGGTTTGTGCCGAACCAGGTGATAGCGGA GGTAGCCTTTTAGCGGGAAATCAAGCCCAAGGTGTCACGTCAGGTGGT TCTGGAAATTGTCGGACGGGGGGAACAACATTCTTTCAACCAGTCAAC CCGATTTTGCAGGCTTACGGCCTGAGAATGATTACGACTGACTCTGGA AGTTCCCCT GCTCCAGCACCTACATCATGTACAGGCTACGCAAGAACG TTCACAGGAACCCTCGCAGCAGGAAGAGCAGCAGCTCAACCGAACGGT AGCTATGTTCAGGTCAACCGGAGCGGTACACATTCCGTCTGTCTCAAT GGACCTAGCGGTGCGGACTTTGATTTGTATGTGCAGCGATGGAATGGC AGTAGCTGGGTAACCGTCGCTCAATCGACATCGCCGGGAAGCAATGAA ACCATTACGTACCGCGGAAATGCTGGATATTATCGCTACGTGGTTAAC GCTGCGTCAGGATCAGGAGCTTACACAATGGGACTCACCCTCCCCTGA

In the above sequence, bold indicates the DNA that encodes the mature protease, standard font indicates the leader sequence, and the underline indicates the N-terminal and C-terminal prosequences. The mature serine protease enzyme derived from Cellulomonas strain 69B4 (DSM 983316035) is 189 amino acids long, with a catalytic triad consisting of His32, Asp56, and Ser137, as shown below (with the catalytic triad indicated in bold and underline):

(SEQ ID NO: 567) FDVIGGNAYT IGGRSRCSIG FAVNGGFITA G H CGRTGATT ANPTGTFAGS SFPGN D YAFV RTGAGVNLLA QVNNYSGGRV QVAGHTAAPV GSAVCRSGST TGWHCGTITA LNSSVTYPEG TVRGLIRTTV CAEPGD S GGS LLAGNQAQGV TSGGSGNCRT GGTTFFQPVN PILQAYGLRM ITTDSGSSP

Example 16 Production of ASP Combinatorial Mutants and Multiple Mutation Libraries

In this Example, methods used to construct combinatorial mutants and multiple mutation libraries of ASP are described. Construction of combinatorial mutants of ASP is described in U.S. patent application Ser. No. 10/576,331.

Multiple Mutation Library Construction

The multiple mutation library was constructed as outlined in the Stratagene QCMS kit, with the exception of the primer concentration used in the reactions. Specifically, 1 μL, of the methylated, purified pUC18-ASP plasmid (about 70 ng) was mixed with 15 μL of sterile distilled water, 1.5 μL of dNTP, 2.5 μL of 10× buffer, 1 μL of the enzyme blend and 1.0 μL mutant primer mix (for a total of 100 μmol of primers). The primer mix was prepared using 10 μL of each of the eighteen mutant primers (100 pmol/μL); adding 50 ng of each primer for the library as recommended by Stratagene, resulted in fewer mutations in a previous round of mutagenesis. Thus, the protocol was modified in the present round of mutagenesis to include a total of 100 pmol of primers in each reaction. The cycling conditions were 95° C. for 1 min, followed by 30 cycles of 95° C. for 1 min, 55° C. for 1 min, and 65° C. for 12 min, in an MJ Research PTC2-200 thermocycler using thin-walled 0.2 mL PCR tubes. The reaction product was digested with 1 μL of DpnI from the QCMS kit by incubating at 37° C. overnight. An additional 0.5 μL of DpnI was added, and the reaction was incubated for 1 hour.

Subsequently, the library DNA (mutagenized single stranded pUC18-ASP product) was electroporated into electrocompetent E. coli cells (Invitrogen®, Catalog No. C4040-52, One Shot® TOP10 Electrocomp™ E. coli, dam+) and growth of transformed cells was selected on agar plates containing 100 mg/L ampicillin resulting in the ASP multiple mutation library in E. coli cells. Colonies (tens of thousands) were harvested and the Qiagen spin miniprep DNA kit (Catalog No. 27106) was used for preparing the plasmid DNA by the steps outlined by the manufacturer. The miniprep DNA was eluted with 50 μL of Qiagen buffer EB provided in the kit.

Miniprep DNA was digested using the PstI and HindIII DNA restriction enzymes. The ASP library fragment mix (PstI x HindIII) was gel purified and cloned in the 4154 basepair HindIII x PstI pHPLT vector fragment by a ligase reaction using Invitrogen® T4 DNA Ligase (Catalog No. 15224-025) as recommended by the manufacturer for cloning cohesive ends). In another approach, synthetic ASP library fragments were produced by GeneArt. These ASP library fragments were also digested with PstI and HindIII, purified and cloned in the 4154 basepair HindIII x PstI pHPLT vector fragment by a ligase reaction.

To transform the ligation reaction mix directly into Bacillus cells, the library DNA (ASP library fragment mix cloned in pHPLT) was amplified using the TempliPhi kit (Amersham Catalog No. 25-6400). For this purpose, 1 μL of the ligation reaction mix was mixed with 5mL of sample buffer from the TempliPhi kit and heated for 3 minutes at 95° C. to denature the DNA. The reaction was placed on ice to cool for 2 minutes and then spun down briefly. Next, 5 μL of reaction buffer and 0.2 μL of phi29 polymerase from the TempliPhi kit were added, and the reactions were incubated at 30° C. in an MJ Research PCR machine for 4 hours. The phi29 enzyme was heat inactivated in the reactions by incubation at 65° C. for 10 min in the PCR machine.

For transformation of the libraries into Bacillus, 0.1 μL of the TempliPhi amplification reaction product was mixed with 500 μL of competent B. subtilis cells (ΔaprE, ΔnprE, oppA, ΔspoIIE, degUHy32, ΔamyE::(xylR,pxylA-comK) followed by vigorous shaking at 37° C. for 1 hour and 100 and 500 μL was plated on HI-agar plates containing 20 ppm neomycin sulfate (Sigma, Catalog No. N-1876; contains 732 μg neomycin per mg) and 0.5% skim milk Ninety-five clones from the library were picked for sequencing.

The mutagenesis worked well, in that only 14% of the clones were equal to the backbone (parent) sequence (ASP with R0141-A064K-T086K-T116E-R123F), and about 3% of clones had extra mutations. The remaining sequenced clones (72%) were all mutants and of these about 94% were unique mutants. The sequencing results for the library are provided below in Table 16-1.

TABLE 16-1 Variants of ASP with R014I-A064K-T086K-T116E-R123F G54D N24A N24Q N24T N67S R127K R159F R159K R159K R159N R159N G78D R159F N24Q R35E N67S R159E R127K R159E R127K R159K R127K R159N R127Q R159K R35D R159E R35D R159K R35E R159K G54D R127K R159K G78D R127K R159K G78D R127K R159E G78D R127Q R159K N24A N67A R159K N24A N67S R159K N24E R35D G78D N24T N67S R159E N67L G78D R159K R35D G78D R159K N24A R35E G78D R159N N24D R35D G78D R159F N24E G54D G78D R159K N24E R35D G78D R127K R159N N24Q G54D G78D R159N N24Q N67L G78D R159E N24Q R35D R127K R159K N24T R35D G78D R159K N24T R35D G78D R159K N67S G78D R127K R159K R35D G78D R127K R159E R35D G78D R127K R159N R35D G78D R127Q R159K R35E G54D N67A R159F R35E N67S G78D R127Q N24A G54D N67S G78D R159F N24A R35D N67A G78D R159F N24Q R35D N67L G78D R159K N24Q R35D N67L G78D R159N N24Q R35D N67S R127K R159E N24Q R35E N67A R127K R159E N24Q R35E N67A G78D R159E N24T N67A G78D R127Q R159N N24T R35E N67A G78D R127Q R35E G54D N67S G78D R159K N24A G54D N67S G78D R127K R159K N24A R35E N67S G78D R127K R159K N24E R35E G54D N67S R127K R159N N24Q R35D N67S G78D R127K R159F N24T G54D N67S G78D R127Y R159E N24E R35E G54D N67S G78D R127K R159K

Example 17 Correlation of Deleterious Mutations for Multiple Properties

In this Example, the principle that deleterious mutations for any property are correlated with deleterious mutations for every other property, regardless of correlations of the properties is exemplified. As indicated herein, only a small number of positions (5-10%) have mutations that are bad for all properties. These positions define the protein fold and are conserved in evolution. The implication of this is that although identification of beneficial mutations for any property requires a truly predictive screen for that property, identification of mutations likely to be deleterious for any property can be accomplished using any screen, including but not limited to the methods provided herein.

The variant enzymes were produced as described herein and within U.S. patent application Ser. Nos. 10/576,331, 10/581,014, 11/581,102, and 11/583,334, all of which are incorporated by reference in their entirety. The tables below provide pair-wise comparisons of the numbers of variants with more than 5% wt activity and less than 5% activity for each of two properties, along with correlation coefficients for the two properties. The assay systems used in this Example are also provided in the above referenced applications. The properties used herein were casein activity (CAS), keratin activity (KER), AAPF activity (AAPF), LAS stability (LAS) and thermal stability for ASP; and peracid formation (PAF) and peracid degradation (PAD) for ACT.

Keratin Hydrolysis Assay

In this assay system, the chemical and reagent solutions used were:

-   Keratin ICN 902111 -   Detergent 1.6 g. detergent was dissolved in 1000 ml water (pH=8.2)     -   0.6 ml. CaCl₂/MgC12 of 10,000 gpg was also added, as well as         1190 mg HEPES, giving a hardness and buffer strength of 6 gpg         and 5 mM respectively. The pH was adjusted to 8.2 with NaOH.     -   Picrylsulfonic acid (TNBS)     -   Sigma P-2297 (5% solution in water) -   Reagent A 45.4 g Na₂B₄O₇.10 H2O (Merck 6308) and 15 ml of 4N NaOH     were dissolved together to a final volume of 1000 ml (by heating if     needed) -   Reagent B 35.2 g NaH₂PO₄1H₂O (Merck 6346) and 0.6 g Na₂SO₃     (Merck 6657) were dissolved together to a final volume of 1000 ml.

Method:

Prior to the incubations, keratin was sieved on a 100 μm sieve in small portions at a time. Then, 10 g of the <100 μm keratin was stirred in detergent solution for at least 20 minutes at room temperature with regular adjustment of the pH to 8.2. Finally, the suspension was centrifuged for 20 minutes at room temperature (Sorvall, GSA rotor, 13,000 rpm). This procedure was then repeated. Finally, the wet sediment was suspended in detergent to a total volume of 200 ml, and the suspension was kept stirred during pipetting. Prior to incubation, MTPs were filled with 200 μl substrate per well with a Biohit multichannel pipette and 1200 μl tip (6 dispenses of 200 μl and dispensed as fast as possible to avoid settling of keratin in the tips). Then, 10 μl of the filtered culture was added to the substrate containing MTPs. The plates were covered with tape, placed in an incubator and incubated at 20° C. for 3 hours at 350 rpm (New Brunswick Innova 4330). Following incubation, the plates were centrifuged for 3 minutes at 3000 rpm (Sigma 6K 15 centrifuge). About 15 minutes before removal of the first plate from the incubator, the TNBS reagent was prepared by mixing 1 ml TNBS solution per 50 ml of reagent A.

MTPs were filled with 60 μl TNBS reagent A per well. From the incubated plates, 10 μl was transferred to the MTPs with TNBS reagent A. The plates were covered with tape and shaken for 20 minutes in a bench shaker (BMG Thermostar) at room temperature and 500 rpm. Finally, 200 μl of reagent B was added to the wells, mixed for 1 minute on a shaker, and the absorbance at 405 nm was measured with the MTP-reader.

Calculation of the Keratin Hydrolyzing Activity

The obtained absorbance value was corrected for the blank value (substrate without enzyme). The resulting absorbance provides a measure for the hydrolytic activity. For each sample (variant) the performance index was calculated. The performance index compares the performance of the variant (actual value) and the standard enzyme (theoretical value) at the same protein concentration. In addition, the theoretical values can be calculated, using the parameters of the Langmuir equation of the standard enzyme. A performance index (PI) that is greater than 1 (PI>1) identifies a better variant as compared to the standard (e.g., wild-type), while a PI of 1 (PI=1) identifies a variant that performs the same as the standard, and a PI that is less than 1 (PI<1) identifies a variant that performs worse than the standard. Thus, the PI identifies winners, as well as variants that are less desirable for use under certain circumstances.

Dimethylcasein Hydrolysis Assay (96 wells)

In this assay system, the chemical and reagent solutions used were:

-   Dimethylcasein (DMC): Sigma C-9801 -   TWEEN®-80: Sigma P-8074 -   PIPES buffer (free acid): Sigma P-1851; 15.1 g was dissolved in     about 960 ml water; pH is adjusted: to 7.0 with 4N NaOH, 1 ml 5%     TWEEN®-80 was added and the volume brought up to 1000 ml. The final     concentration of PIPES and TWEEN®-80 is 50 mM and 0.005%     respectively. -   Picrylsulfonic acid (TNBS): Sigma P-2297 (5% solution in water) -   Reagent A: 45.4 g Na₂B₄O₇.10 H2O (Merck 6308) and 15 ml of 4N NaOH     dissolved together to a final volume of 1000 ml (by heating if     needed) -   Reagent B: 35.2 g NaH₂PO₄.1H₂O (Merck 6346) and 0.6 g Na₂SO₃     (Merck 6657) dissolved together to a final volume of 1000 ml.

Method:

To prepare the substrate, 4 g DMC were dissolved in 400 ml PIPES buffer. The filtered culture supernatants were diluted with PIPES buffer; the final concentration of the controls in the growth plate was 20 ppm. Then, 10 μl of each diluted supernatant were added to 200 μl substrate in the wells of a MTP. The MTP plate was covered with tape, shaken for a few seconds and placed in an oven at 37° C. for 2 hours without agitation.

About 15 minutes before removal of the first plate from the oven, the TNBS reagent was prepared by mixing 1 ml TNBS solution per 50 ml of reagent A. MTPs were filled with 60 μl TNBS reagent A per well. The incubated plates were shaken for a few seconds, after which 10 μl were transferred to the MTPs with TNBS reagent A. The plates were covered with tape and shaken for 20 minutes in a bench shaker (BMG Thermostar) at room temperature and 500 rpm. Finally, 200 μl of reagent B were added to the wells, mixed for 1 minute on a shaker, and the absorbance at 405 nm was determined using an MTP reader.

Calculation of Dimethylcasein Hydrolyzing Activity:

The obtained absorbance value was corrected for the blank value (substrate without enzyme). The resulting absorbance is a measure for the hydrolytic activity. The (arbitrary) specific activity of a sample was calculated by dividing the absorbance and the determined protein concentration.

Thermostability Assay

This assay is based on the dimethylcasein (DMC) hydrolysis, before and after heating of the buffered culture supernatant. The same chemical and reagent solutions were used as described in the DMC hydrolysis assay.

Method:

The filtered culture supernatants were diluted to 20 ppm in PIPES buffer (based on the concentration of the controls in the growth plates). Then, 50 μl of each diluted supernatant were placed in the empty wells of a MTP. The MTP plate was incubated in an iEMS incubator/shaker HT (Thermo Labsystems) for 90 minutes at 60° C. and 400 rpm. The plates were cooled on ice for 5 minutes. Then, 10 μl of the solution was added to a fresh MTP containing 200 μl DMC substrate/well. This MTP was covered with tape, shaken for a few seconds and placed in an oven at 37° C. for 2 hours without agitation. The same detection method as used for the DMC hydrolysis assay was employed.

Calculation of Thermostability:

The residual activity of a sample was expressed as the ratio of the final absorbance and the initial absorbance, both corrected for blanks.

As indicated in the following Tables, the only properties that were found to be correlated (correlation coefficients >0.5) were CAS, KER and AAPF for ASP. All of the others were not correlated (correlation coefficient <0.3). In spite of the fact that the properties were not correlated, the probability that a mutation would be deleterious for the two properties is much higher than expected by chance. Table 17-1 provides the calculated ratios of observed numbers of variants, and expected numbers of variants based on chance. Numbers that are greater than 1 indicate positive correlations, and numbers that are less than 1 indicate negative correlations.

TABLE 17-1 CAS and KER Comparison Results for ASP Observed Expected Observed/ Value CAS KER CAS KER Expected <=5% 892 674         31% 24% >5% 1959 2177         69% 76% both >5% 1877 66% 1496 52% 1.25 one >5% 382 13% 1144 40% 0.33 Both <=5% 592 21%  211  7% 2.81 at least one >5% 2259 79% 2640 93% 0.86

TABLE 17-2 CAS and AAPF Comparison Results for ASP Observed Expected Observed/ Value CAS AAPF CAS AAPF Expected <=5% 892 1263         31% 44% >5% 1959 1588         69% 56% both >5% 1576 55% 1091 38% 1.44 one >5% 395 14% 1365 48% 0.29 Both <=5% 880 31%  395 14% 2.23 at least one >5% 1971 69% 2456 86% 0.80

TABLE 17-3 CAS and LAS Comparison Results for ASP Observed Expected Observed/ Value CAS LAS CAS LAS Expected <=5% 892 1450         31% 51% >5% 1959 1401         69% 49% both >5% 1393 49%  963 34% 1.45 one >5% 574 20% 1435 50% 0.40 Both <=5% 884 31%  454 16% 1.95 at least one >5% 1967 69% 2397 84% 0.82

TABLE 17-4 CAS and Thermal Stability Comparison Results for ASP Observed Expected Observed/ Value CAS THER CAS THER Expected <=5% 892 1198         31% 42% >5% 1959 1653         69% 58% both >5% 1508 53% 1136 40% 1.33 one >5% 596 21% 1340 47% 0.44 Both <=5% 747 26%  375 13% 1.99 at least one >5% 2104 74% 2476 87% 0.85

TABLE 17-5 KER and AAPF Comparison Results for ASP Observed Expected Observed/ Value KER AAPF KER AAPF Expected <=5% 674 1263         24% 44% >5% 2177 1588         76% 56% both >5% 1566 55% 1213 43% 1.29 one >5% 633 22% 1340 47% 0.47 Both <=5% 652 23%  299 10% 2.18 at least one >5% 2199 77% 2552 90% 0.86

TABLE 17-6 PAF and PAD Comparison Results for ACT Observed Expected Value PAF PAD PAF PAD Observed/Expected <=5% 541  751 19% 26% >5% 2536 2326 89% 82% both >5% 2187 77% 2069 73% 1.06 one >5% 488 17% 639 22% 0.76 Both <=5% 402 14% 143 5% 2.82 at least one >5% 2675 94% 2708 95% 0.99 

1. An isolated subtilisin variant of a Bacillus subtilisin, wherein said subtilisin variant is a mature form having proteolytic activity and comprising a substitution at one or more positions selected from: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 33, 35, 36, 37, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 64, 65, 66, 67, 71, 72, 73, 76, 77, 78, 79, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 101, 102, 103, 104, 105, 106, 107, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 122, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 139, 141, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 156, 157, 158, 159, 160, 162, 163, 164, 165, 166, 167, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 194, 195, 196, 197, 198, 199, 200, 201, 203, 204, 206, 207, 209, 210, 212, 213, 214, 215, 216, 217, 218, 219, 220, 222, 223, 224, 225, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 267, 268, 269, 270, 271, 272, 273 and 274, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 2. The isolated subtilisin variant of claim 1, wherein said one or more positions is selected from: 1, 2, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 21, 22, 23, 24, 25, 26, 28, 29, 30, 31, 33, 35, 36, 37, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 64, 65, 66, 67, 71, 72, 73, 77, 78, 79, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 101, 102, 103, 104, 105, 106, 107, 109, 110, 111, 112, 113, 114, 115, 116, 118, 119, 122, 124, 125, 126, 127, 128, 129, 131, 133, 134, 135, 136, 137, 139, 141, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 156, 157, 158, 159, 160, 162, 163, 164, 165, 166, 167, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 194, 195, 196, 197, 198, 199, 200, 201, 203, 204, 206, 207, 212, 213, 214, 215, 216, 217, 218, 219, 220, 222, 223, 224, 225, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, 250, 251, 253, 254, 255, 256, 257, 258, 259, 260, 261, 262, 263, 264, 265, 267, 268, 269, 270, 271, 272, 273 and 274, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 3. The subtilisin variant of claim 1, wherein said one or more positions are selected from 2, 3, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 19, 20, 21, 21, 22, 23, 25, 26, 28, 29, 30, 31, 33, 35, 36, 37, 39, 40, 41, 42, 44, 46, 47, 48, 49, 50, 51, 53, 54, 55, 56, 57, 58, 59, 60, 64, 65, 66, 67, 71, 73, 77, 78, 79, 81, 82, 83, 84, 85, 86, 88, 89, 90, 91, 92, 93, 94, 95, 96, 102, 105, 106, 110, 111, 112, 113, 114, 115, 116, 122, 124, 125, 128, 129, 131, 133, 134, 135, 136, 137, 139, 141, 143, 145, 146, 147, 148, 149, 150, 151, 152, 153, 156, 157, 158, 159, 160, 162, 165, 166, 167, 169, 170, 171, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 186, 187, 189, 190, 191, 192, 194, 195, 196, 197, 198, 199, 200, 201, 203, 204, 206, 207, 212, 214, 216, 217, 218, 219, 220, 222, 223, 224, 225, 228, 229, 230, 231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 249, 250, 251, 253, 254, 255, 257, 258, 259, 260, 261, 262, 263, 264, 265, 267, 268, 269, 270, 271, 272, 273, and 274, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 4. The subtilisin variant of claim 1, wherein said subtilisin variant further comprises a substitution at one or more positions selected from the group consisting of: 18, 52, 72, 117, 119, 127, 144, 185, 209 and 213, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 5. The subtilisin variant of claim 1, wherein said substitution comprises one or more of: A001C, A001D, A001E, A001F, A001G, A001H, A001I, A001K, A001L, A001M, A001N, A001Q, A001R, A001S, A001V, A001W, Q002A, Q002D, Q002E, Q002G, Q002S, S003A, S003D, S003F, S003G, S003I, S003K, S003L, S003M, S003N, S003P, S003Q, S003R, S003T, S003V, S003W, S003Y, P005C, P005E, P005G, P005N, P005Q, P005T, Y006A, Y006C, Y006E, Y006F, Y006G, Y006K, Y006M, Y006N, Y006P, Y006Q, Y006R, Y006T, Y006V, Y006W, S009A, S009C, S009E, S009F, S009G, S009H, S009K, S009L, S009M, S009P, S009Q, S009R, S009T, S009V, S009W, Q010A, Q010C, Q010E, Q010F, Q010G, Q010H, Q010I, Q010K, Q010L, Q010M, Q010R, Q010S, Q010T, Q010V, Q010W, I011C, I011L, I011T, I011V, I011Y, K012A, K012C, K012D, K012E, K012F, K012G, K012H, K012I, K012N, K012Q, K012S, K012T, K012V, K012W, K012Y, A013C, A013F, A013G, A013H, A013L, A013R, A013S, A013T, A013V, P014A, P014C, P014D, P014E, P014F, P014G, P014I, P014K, P014L, P014M, P014N, P014Q, P014R, P014S, P014T, P014V, P014W, P014Y, A015C, A015D, A015E, A015F, A015G, A015H, A015I, A015K, A015L, A015M, A015P, A015Q, A015R, A015T, A015V, A015Y, L016A, L016C, L016I, L016M, L016Q, L016S, L016T, H017F, H017I, H017L, H017M, H017V, H017W, H017Y, S018A, S018E, S018F, S018G, S018H, S018I, S018K, S018L, S018M, S018N, S018P, S018Q, S018R, S018T, S018V, S018W, S018Y, Q019A, Q019C, Q019D, Q019E, Q019G, Q019I, Q019K, Q019M, Q019R, Q019T, Q019V, G020A, G020C, G020D, G020E, G020F, G020H, G020K, G020M, G020N, G020P, G020Q, G020R, G020S, G020W, Y021A, Y021C, Y021D, Y021E, Y021F, Y021G, Y021H, Y021K, Y021M, Y021R, Y021S, Y021T, Y021V, Y021W, T022A, T022C, T022E, T022F, T022G, T022H, T022I, T022K, T022L, T022M, T022N, T022Q, I022S, T022V, I022W, T022Y, S024C, S024F, S024G, S024H, S024I, S024K, S024L, S024M, S024N, S024Q, S024R, S024T, S024W, S024Y, N025C, N025E, N025F, N025G, N025H, N025I, N025K, N025L, N025M, N025P, N025R, N025S, N025T, N025V, N025W, K027A, K027D, K027E, K027F, K027G, K027H, K027L, K027M, K027P, K027R, K027S, K027W, K027Y, D032A, D032C, D032E, D032G, D032I, D032K, D032L, D032M, D032N, D032R, D032S, D032T, D032V, D032Y, S033A, S033F, S033G, S033H, S033P, S033T, S033W, I035A, I035C, I035D, I035R, I035S, I035T, I035V, D036A, D036C, D036E, D036Q, D036S, D036W, S037A, S037C, S037E, S037F, S037G, S037H, S037K, S037L, S037M, S037P, S037Q, S037R, S037T, S037W, H039C, H039Q, H039T, H039V, P040A, P040C, P040E, P040F, P040G, P040G, P040H, P040I, P040K, P040L, P040M, P040N, P040Q, P040R, P040S, P040T, P040V, P040W, D041E, L042I, L042M, L042V, K043A, K043C, K043D, K043E, K043F, K043G, K043I, K043L, K043M, K043N, K043R, K043S, K043T, K043V, K043W, K043Y, V044A, V044C, V044I, V044L, V044M, V044P, V044S, V044T, A045C, A045E, A045F, A045H, A045I, A045K, A045L, A045M, A045N, A045P, A045Q, A045S, A045T, A045V, A045Y, G046A, G046C, G046E, G046H, G046K, G046M, G046N, G046Q, G046T, G046W, G046Y, A048C, A048D, A048E, A048F, A048H, A048I, A048K, A048L, A048M, A048Q, A048R, A048S, A048T, A048V, A048W, A048Y, M050A, M050C, M050F, M050H, M050I, M050K, M050L, M050Q, M050R, M050S, M050T, M050V, M050W, M050Y, V051A, V051C, V051D, V051E, V051H, V051I, V051L, V051P, V051Q, P052C, P052D, P052E, P052F, P052H, P052I, P052K, P052L, P052Q, P052R, P052S, P052T, P052V, P052W, P052Y, S053E, S053F, S053G, S053H, S053I, S053K, S053L, S053M, S053N, S053Q, S053R, S053T, S053V, S053W, E054A, E054N, E054Q, E054S, T055A, T055C, T055D, T055F, T055G, T055H, T055I, T055K, T055M, T055P, T055Q, T055R, T055S, T055V, T055W, T055Y, N056D, N056M, N056P, N056Q, N056S, N056T, N056V, P057N, P057Q, P057T, P057V, P057W, F058C, F058E, F058G, F058H, F058L, F058M, F058N, F058Q, F058S, F058V, F058Y, Q059A, Q059C, Q059D, Q059E, Q059F, Q059G, Q059H, Q059K, Q059L, Q059M, Q059N, Q059P, Q059R, Q059S, Q059T, Q059V, Q059W, Q059Y, D060E, D060G, H064C, H064D, H064F, H064I, H064L, H064M, H064Q, H064R, H064S, H064T, H064V, H064Y, T066S, T066W, T066Y, H067A, H067C, H067F, H067I, H067L, H067M, H067N, H067P, H067R, H067S, H067T, T071I, T071Y, N077S, S078A, S078C, S078D, S078F, S078G, S078I, S078K, S078L, S078M, S078N, S078P, S078Q, S078R, S078T, S078V, S078W, S078Y, I079A, I079C, I079E, I079F, I079G, I079H, I079K, I079L, I079N, I079Q, I079R, I079S, I079T, I079V, I079W, I079Y, V081F, V081I, V081L, V081M, V081T, G083F, G083P, Q084A, Q084C, Q084H, Q084I, Q084N, Q084T, A085C, A085F, A085G, A085R, A085S, P086A, P086D, P086E, P086G, P086M, P086N, P086Q, P086R, P086S, P086T, P086W, P086Y, S089C, S089D, S089E, S089F, S089G, S089H, S089K, S089L, S089V, S089W, S089Y, L090A, L090D, L090E, L090G, L090H, L090M, L090Q, L090T, L090V, Y091A, Y091C, Y091D, Y091E, Y091F, Y091H, Y091I, Y091L, Y091M, Y091Q, Y091S, Y091T, Y091V, L096F, L096H, L096I, L096K, L096M, L096T, L096V, G097A, G097C, G097D, G097E, G097H, G097K, G097L, G097M, G097P, G097Q, G097R, G097S, G097T, G097V, A098C, A098D, A098F, A098G, A098H, A098I, A098L, A098P, A098Q, A098R, A098S, A098T, A098V, A098Y, D099C, D099E, D099I, D099K, D099L, D099N, D099P, D099Q, D099R, D099S, D099T, S101A, S101C, S101E, S101F, S101G, S101I, S101K, S101L, S101M, S101N, S101P, S101Q, S101R, S101T, S101V, S101Y, G102A, G102C, G102E, G102F, G102I, G102N, G102S, G102V, G102Y, Q103A, Q103C, Q103E, Q103F, Q103G, Q103I, Q103K, Q103L, Q103M, Q103N, Q103R, Q103S, Q103T, Q103V, Q103W, S105A, S105C, S105D, S105E, S105F, S105G, S105I, S105K, S105L, S105M, S105N, S105P, S105R, S105V, S105W, W106A, W106C, W106E, W106F, W106G, W106H, W106I, W106L, W106M, W106N, W106R, W106S, W106T, W106V, W106Y, N109A, N109C, N109E, N109F, N109G, N109H, N109L, N109M, N109P, N109Q, N109R, N109S, N109T, N109V, N109W, N109Y, I111C, I111F, I111L, I111M, I111N, I111P, I111T, I111V, I111W, E112A, E112C, E112D, E112F, E112G, E112I, E112L, E112M, E112N, E112Q, E112R, E112S, E112T, E112V, E112W, E112Y, W113D, W113E, W113F, W113N, W113P, W113Q, W113S, W113V, W113Y, I115E, I115H, I115N, I115R, I115T, I115V, I115W, I115Y, A116C, A116D, A116E, A116F, A116G, A116H, A116I, A116K, A116L, A116M, A116N, A116P, A116Q, A116R, A116S, A116T, A116V, A116W, A116Y, N118A, N118C, N118D, N118E, N118F, N118G, N118H, N118I, N118K, N118L, N118M, N118Q, N118R, N118S, N118T, N118V, N118W, N118Y, I122A, I220, I122H, I122K, I122L, I122M, I122N, I122P, M124C, M124D, M124I, M124L, M124S, M124T, M124V, M124W, S125A, S125C, S125E, S125F, S125I, S125K, S125M, S125N, S125P, S125Q, S125R, S125T, S125W, L126A, L126C, L126I, L126K, L126N, L126R, L126S, L126T, L126V, L126W, L126Y, G127A, G127C, G127E, G127F, G127I, G127K, G127M, G127N, G127P, G127Q, G127S, G127T, G127V, G127W, G127Y, G128A, G128D, G128F, G128H, G128L, G128N, G128P, G128S, G128T, G128V, G128W, G128Y, P129A, P129C, P129D, P129E, P129F, P129G, P129I, P129K, P129L, P129M, P129N, P129Q, P129S, P129T, P129V, P129Y, G131A, G131C, G131E, G131F, G131K, G131L, G131M, G131N, G131P, G131Q, G131R, G131S, G131T, G131V, G131W, G131Y, A133C, A133D, A133E, A133F, A133G, A133I, A133K, A133L, A133M, A133P, A133R, A133S, A133T, A133V, A133W, A133Y, A134D, A134E, A134F, A134G, A134I, A134K, A134L, A134M, A134P, A134Q, A134R, A134S, A134I, A134V, A134W, L135D, L135E, L135M, L135R, L135W, L135Y, K136E, K136H, K136L, K136M, K136N, K136R, K136S, K136T, K136V, K136W, K136Y, A137C, A137E, A137F, A137H, A137K, A137L, A137M, A137N, A137P, A137Q, A137R, A137S, A137T, A137V, A137W, A137Y, V139C, V139I, V139L, V139N, V139S, V139T, K141A, K141C, K141D, K141E, K141F, K141G, K141H, K141I, K141L, K141M, K141N, K141Q, K141R, K141S, K141V, K141W, K141Y, V143A, V143C, V143D, V143E, V143F, V143G, V143K, V143L, V143M, V143N, V143Q, V143R, V143S, V143T, V143W, A144C, A144D, A144E, A144G, A144I, A144K, A144L, A144M, A144R, A144S, A144T, A144V, A144W, S145A, S145C, S145D, S145E, S145F, S145G, S145H, S145I, S145L, S145M, S145Q, S145R, S145T, S145V, S145W, S145Y, G146A, G146C, G146D, G146E, G146M, G146Q, G146R, G146S, G146T, G146Y, A153S, G154L, G154P, G154T, E156A, E156C, E156F, E156K, E156L, E156N, E156Q, E156R, E156S, E156T, E156V, E156W, E156Y, T158A, T158D, T158E, I158G, T158H, I158I, T158K, T158L, T158M, T158N, T158Q, T158S, T158V, T158Y, S159A, S159C, S159D, S159E, S159G, S159H, S159I, S159K, S159M, S159Q, S159R, S159T, G160D, G160E, G160K, G160N, G160P, G160Q, G160S, G160T, S162A, S162C, S162E, S162H, S162K, S162L, S162M, S162N, S162Q, S162R, S162T, S162V, S163G, S163P, Y167A, Y167F, Y167H, Y167I, P168D, P168G, P168I, P168M, P168S, P168Y, G169A, G169E, G169F, G169H, G169I, G169M, G169N, G169R, G169T, G169V, G169Y, K170A, K170C, K170F, K170G, K170H, K170R, K170V, K170W, K170Y, Y171G, Y171K, Y171P, P172A, P172C, P172E, P172K, P172L, P172M, P172N, P172Q, P172R, P172S, P172T, P172V, P172Y, S173A, S173C, S173E, S173I, S173T, S173V, V174C, V174F, V174H, V174R, V174T, I175G, I175L, I175M, I175R, I175T, I175V, A176C, A176E, A176F, A176K, A176M, A176S, A176Y, A179G, V180A, V180C, V180L, V180N, V180S, V180T, D181C, D181E, D181G, D181H, D181M, D181N, D181S, D181T, D181W, S182A, S182C, S182D, S182F, S182G, S182H, S182I, S182K, S182M, S182P, S182Q, S182R, S182V, S182Y, S183A, S183C, S183E, S183F, S183G, S183H, S183I, S183K, S183L, S183M, S183N, S183Q, S183R, S183T, S183V, S183W, S183Y, N184C, N184D, N184E, N184G, N184H, N184K, N184L, N184M, N184Q, N184S, N184T, N184V, N184W, Q185A, Q185C, Q185E, Q185F, Q185G, Q185H, Q185I, Q185K, Q185L, Q185M, Q185N, Q185S, Q185T, Q185V, Q185W, R186I, R186L, R186W, A187C, A187D, A187E, A187F, A187G, A187P, A187S, A187W, A187Y, S188A, S188C, S188D, S188E, S188F, S188G, S188H, S188I, S188K, S188L, S188M, S188P, S188Q, S188T, S188V, S188W, S188Y, S190F, S190H, S190I, S190K, S191A, S191G, S191N, S191P, V192A, V192S, V192T, V192Y, G193F, G193H, G193I, G193N, G193P, G193R, G193T, P194C, P194E, P194H, P194I, P194K, P194L, P194M, P194Q, P194T, P194V, P194W, L196A, M199P, M199S, A200C, A200G, A200K, A200Y, G202D, G202E, G202F, G202L, G202P, G202V, G202Y, Q206A, Q206C, Q206D, Q206E, Q206F, Q206G, Q206H, Q206I, Q206L, Q206M, Q206N, Q206P, Q206R, Q206S, Q206T, Q206V, Q206W, Q206Y, S207D, S207E, S207K, S207Q, S207T, S207V, P210A, P210C, P210S, P210T, N212A, N212C, N212E, N212F, N212G, N212H, N212K, N212L, N212M, N212P, N212Q, N212R, N212S, N212V, K213A, K213C, K213D, K213E, K213F, K213H, K213I, K213L, K213M, K213N, K213Q, K213R, K213S, K213T, K213V, K213Y, Y214W, G215A, G215C, G215D, G215E, G215I, G215M, G215N, G215Q, G215S, G215T, G215V, A216C, A216D, A216E, A216G, A216K, A216L, A216M, A216N, A216P, A216Q, A216R, A216S, A216V, A216W, Y217A, Y217C, Y217D, Y217E, Y217F, Y217G, Y217H, Y217I, Y217K, Y217L, Y217M, Y217N, Y217Q, Y217R, Y217S, Y217T, Y217V, Y217W, N218A, N218C, N218E, N218F, N218G, N218H, N218K, N218M, N218R, N218S, N218T, N218W, N218Y, G219A, G219C, G219D, G219H, G219I, G219M, G219P, G219Q, G219R, G219S, G219T, G219V, G219W, T220D, T220E, T220F, T220G, T220K, T220M, T220S, T220Y, A223E, A223F, A223L, A223M, A223R, A223S, A223V, A223W, A223Y, S224A, S224C, S224F, S224G, S224H, S224M, S224N, S224Q, S224R, S224T, P225A, P225C, P225F, P225G, P225H, P225I, P225K, P225L, P225M, P225R, P225S, P225I, P225V, P225Y, A228P, A228R, A228S, A228T, A228W, G229A, G229H, G229I, G229S, A230C, A230E, A230G, A230Q, A230R, A230S, A230T, A230V, A231C, A231I, A231P, A231R, I234A, I234C, I234L, I234M, I234N, I234P, I234Q, I234S, I234T, I234V, L235A, L235C, L235G, L235I, L235K, L235M, L235N, L235Q, L235R, L235S, L235T, L235V, L235W, L235Y, S236A, S236C, S236D, S236E, S236G, S236H, S236N, S236Q, S236T, S236V, S236Y, K237A, K237E, K237F, K237G, K237H, K237I, K237L, K237M, K237N, K237Q, K237R, K237S, K237T, K237V, K237W, K237Y, H238C, H238D, H238E, H238F, H238M, H238R, H238S, P239C, P239D, P239E, P239F, P239H, P239L, P239M, P239N, P239Q, P239R, P239S, P239T, P239V, P239W, P239Y, N240A, N240C, N240D, N240F, N240G, N240K, N240L, N240Q, N240R, N240S, N240T, N240V, N240W, N240Y, W241A, W241F, W241G, W241H, W241I, W241K, W241M, W241Q, W241T, W241V, T242A, T242C, T242E, T242F, T242G, T242K, T242M, T242N, T242P, T242R, T242S, T242W, T242Y, N243C, N243E, N243F, N243G, N243I, N243Q, N243S, N243T, N243V, N243W, N243Y, T244A, T244D, T244F, T244G, T244H, T244K, T244L, T244M, T244N, T244P, T244Q, T244R, T244S, T244V, T244W, T244Y, Q245A, Q245C, Q245D, Q245E, Q245H, Q245I, Q245K, Q245L, Q245M, Q245R, Q245T, Q245V, Q245Y, R247W, S248A, S248E, S248F, S248G, S248H, S248I, S248L, S248M, S248N, S248Q, S248R, S248T, S248V, S248W, S248Y, S249C, S249D, S249H, S249I, S249K, S249L, S249M, S249N, S249Q, S249R, S249T, S249V, S249W, S249Y, L250D, L250F, L250H, L250I, L250M, L250T, L250V, E251A, E251T, E251W, N252A, N252C, N252E, N252G, N252H, N252I, N252L, N252M, N252Q, N252R, N252S, N252T, N252V, N252Y, T253A, T253C, T253E, T253G, T253H, T253K, T253M, T253S, T253V, T254A, T254C, T254L, T254M, T254R, T254S, T254V, T255A, T255C, T255D, T255E, T255F, T255G, T255H, T255I, T255K, T255L, T255M, T255R, T255S, T255V, K256A, K256C, K256D, K256E, K256F, K256H, K256I, K256L, K256M, K256N, K256P, K256Q, K256R, K256S, K256T, K256V, K256W, K256Y, L257A, L257C, L257F, L257G, L257H, L257I, L257K, L257M, L257N, L257R, L257S, L257T, L257V, L257W, L257Y, G258Q, D259A, D259E, D259F, D259G, D259L, D259N, D259P, D259Q, D259R, D259S, D259T, D259V, D259W, D259Y, S260A, S260C, S260D, S260E, S260F, S260G, S260H, S260L, S260M, S260N, S260P, S260R, S260V, S260W, S260Y, F261H, F261W, Y262A, Y262C, Y262E, Y262F, Y262H, Y262L, Y262M, Y262N, Y263F, Y263M, Y263T, G264F, G264I, G264L, K265A, K265C, K265E, K265G, K265H, K265L, K265M, K265N, K265Q, K265R, K265S, K265W, K265Y, G266C, G266F, G266L, G266M, G266P, G266R, G266V, G266W, G266Y, L267A, L267C, L267E, L267G, L267H, L267I, L267M, L267N, L267Q, L267S, L267T, L267V, I268A, I268C, I268K, I268L, I268M, I268P, I268R, I268V, N269D, N269E, N269K, N269L, N269P, N269Q, N269S, Q271A, Q271C, Q271D, Q271E, Q271F, Q271G, Q271H, Q271I, Q271K, Q271L, Q271M, Q271N, Q271P, Q271R, Q271S, Q271T, Q271V, Q271W, Q271Y, A272E, A272F, A272G, A272H, A272K, A272L, A272M, A272N, A272Q, A272R, A272S, A272T, A272V, A272W, A272Y, A274C, A274D, A274F, A274G, A274H, A274I, A274K, A274L, A274Q, A274S, A274T, and A274V, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 6. The subtilisin variant of claim 1, wherein said substitution comprises a combination of substitutions selected from: Y021H-Y217E, Y021H-Y217Q, S101E-Y217L, Y021H-Y217L, K213I-Y217Q, A045I-Y217Q, M119F-Y217Q, A045V-Y217L, Y021H-Y217L, K213I-Y217E, A092G-A114G, Y021W-S101E, V26Q-K213I, and Y021H-S101N, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 7. The subtilisin variant of claim 1, wherein said substitution comprises a combination selected from: S101 N-K213I, S101N-M119H, K213L, M119N-K213N, K213N, K213I-Y217E, M119N-K213I, K213N-Y217Q, M119H-K213N, S101P-K213N, M119H-Y217Q, K213I-Y217Q, M119F-K213L, Y217Q, M119F-Y217Q, A048E-K213L, A048H-K213L, K213N, V026N-K213L, V026N-K213L, V026Y-K213N, A048D-K213N, A048H-K213N, A048H-K213L, K213L, K213N, V147D-K213L, K213I, A048E-K213L, A048D-K213N, K213I, A048H-K213N, V147D-K213N, Y021H-Y217L, Y021H-Y217Q, A045V-Y217L, S101E-Y217L, Y021H-Y217E, A045I-Y217Q, Y021H-Y217L, Y021H-Y217E, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 8. The subtilisin variant of claim 1, wherein said substitution comprises a combination selected from: S101N-M119H, Y217L, M119N-K213N, S101E-Y217L, A045I-Y217Q, wherein said positions correspond to the amino acid sequence of B. amyloliquefaciens subtilisin BPN′ set forth as SEQ ID NO:2.
 9. An isolated nucleic acid encoding the subtilisin variant set forth in claim
 1. 10. An expression vector comprising the nucleic acid of claim
 9. 11. A host cell comprising the expression vector set forth claim
 10. 12. A cleaning composition comprising the subtilisin variant of claim
 1. 13. The cleaning composition of claim 12, wherein said cleaning composition is a laundry detergent.
 14. The cleaning composition of claim 13, wherein said laundry detergent is a cold water detergent, a low pH detergent, or a compact detergent.
 15. A method for producing a subtilisin variant of a Bacillus subtilisin, comprising the steps: a) transforming a host cell with an expression vector comprising a nucleic acid encoding the subtilisin variant of claim 1; and b) cultivating the transformed host cell under conditions suitable for the production of the subtilisin variant, to produce a subtilisin variant.
 16. The method of claim 15, further comprising the step of harvesting the produced subtilisin variant.
 17. The method of claim 15, wherein said host cell is a Bacillus species.
 18. The method of claim 17, wherein said Bacillus species is B. subtilis.
 19. A method of cleaning, comprising the step of contacting a surface and/or an article comprising a fabric with a cleaning composition comprising an isolated subtilisin variant of claim
 1. 20. A method for protease engineering comprising: a) providing a plurality of site evaluation libraries (SELs) each comprising a plurality of protease variants having distinct substitutions at an identical amino acid position of said protease; b) testing said protease variants of said SELs and a standard protease in a test of a property of interest; c) determining a performance index (PI) for each of said protease variants for said test; d) identifying two or more of said amino acid positions as non-restrictive positions, wherein at least one of said plurality of protease variants in each of two of said SELs has a PI greater than 0.5; and f) providing a multiple mutation library comprising a plurality of multiply-substituted protease variants each comprising substitutions in said two or more non-restrictive positions.
 21. The method of claim 20, wherein said test comprises two or more different assays selected from the group consisting of stain removal assays (microswatch), LAS stability, EDTA stability, detergent stability assays, and specific activity assays.
 22. The method of claim 20, wherein said protease is a bacterial subtilisin.
 23. A method for producing a multiply substituted subtilisin variant of a Bacillus subtilisin, comprising: a) testing a plurality of singly-substituted subtilisin variants in a first test of a first property and a second test of a second property, wherein the property of a parent subtilisin is given a value of 1.0 in each test, a favorable first or second property has a value greater than 1.0, and an unduly unfavorable first or second property has a value less than about 0.80 or in some preferred embodiments, less than about 0.60; b) identifying a substitution in at least one of the singly-substituted subtilisin variants that is associated with a favorable first property and which is not associated with an unduly unfavorable second property; c) identifying a substitution in at least one of the singly-substituted subtilisin variants that is associated with a favorable second property and which is not associated with an unduly unfavorable first property; d) introducing the substitution from the previous steps into a subtilisin to yield a multiply-substituted subtilisin variant.
 24. The method of claim 23, further comprising testing the multiply-substituted subtilisin variant in the first test and the second test, wherein an improved subtilisin variant achieves a value of greater than 1.0 in both of said first and second tests, or a value of greater than 1.0 in the first test and a value of 0.80 to 1.0 in the second test.
 25. The method of claim 24, further comprising producing the improved subtilisin variant(s).
 26. The method of claim 25, wherein said first and second properties are negatively correlated.
 27. The method of claim 26, wherein a favorable first or second property has a value greater than about 1.2.
 28. The method of claim 24, wherein an unduly unfavorable first or second property has a value less than about 0.40.
 29. The method of claim 24, wherein the first property is stability, and the second property is wash performance.
 30. The method of claim 29, wherein said stability comprises stability in detergent and said wash performance comprises blood milk ink (BMI) wash performance in detergent.
 31. The method of claim 24, wherein wash performance is tested in a powder or liquid detergent composition having a pH of between 5 and 12.0.
 32. The method of claim 24, wherein the parent bacterial subtilisin is a wild type mature form of a B. amyloliquefaciens subtilisin BPN′ having an amino acid sequence set forth as SEQ ID NO:2.
 33. The method of claim 24, wherein the positions are in a parent subtilisin having a solvent accessible surface (SAS) of greater than about 50%.
 34. The method of claim 33, wherein said one or more positions in a parent subtilisin are positions having a solvent accessible surface (SAS) of greater than about 65%. 